Pages that link to "Q657516"
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The following pages link to hereditary spastic paraplegia (Q657516):
Displayed 50 items.
- Hereditary spastic paraplegia type 11 (Q2308009) (← links)
- hereditary spastic paraplegia 4 (Q2308013) (← links)
- (Q3281306) (redirect page) (← links)
- hereditary spastic paraplegia 7 (Q3363626) (← links)
- Troyer syndrome (Q3508706) (← links)
- hereditary spastic paraplegia 23 (Q4664694) (← links)
- Fitzsimmons–Guilbert syndrome (Q5455731) (← links)
- L1 syndrome (Q6714500) (← links)
- mast syndrome (Q18966121) (← links)
- Charcot-Marie-tooth disease type 5 (Q21124579) (← links)
- Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin (Q24295115) (← links)
- Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance (Q24295258) (← links)
- Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia (Q24299953) (← links)
- Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia (Q24301499) (← links)
- Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 (Q24301516) (← links)
- Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network (Q24301595) (← links)
- Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12 (Q24308745) (← links)
- Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia (Q24310003) (← links)
- Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia (Q24317205) (← links)
- A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2 (Q24337836) (← links)
- A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia (Q24338151) (← links)
- The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype (Q24531747) (← links)
- NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6) (Q24532801) (← links)
- Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia (Q24533436) (← links)
- Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegia (Q24534210) (← links)
- A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3 (Q24539096) (← links)
- Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q (Q24540118) (← links)
- A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity (Q24540152) (← links)
- Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60 (Q24563811) (← links)
- Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin (Q24597228) (← links)
- A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10) (Q24632247) (← links)
- Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations (Q24654250) (← links)
- Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31 (Q24669559) (← links)
- Spastin gene mutation in Japanese with hereditary spastic paraplegia (Q24678909) (← links)
- Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia (Q24680886) (← links)
- Tau missorting and spastin-induced microtubule disruption in neurodegeneration: Alzheimer Disease and Hereditary Spastic Paraplegia (Q26774045) (← links)
- Clinical features and management of hereditary spastic paraplegia (Q27026288) (← links)
- Psychometric properties of functional mobility tools in hereditary spastic paraplegia and other childhood neurological conditions (Q27028017) (← links)
- The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8. (Q27301370) (← links)
- A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system (Q27318572) (← links)
- Hereditary spastic paraplegia SPG4: what is known and not known about the disease (Q27690406) (← links)
- The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria (Q27931873) (← links)
- Induced knockouts provide insights into human L1 syndrome (Q28066836) (← links)
- Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia (Q28115985) (← links)
- Protrudin regulates endoplasmic reticulum morphology and function associated with the pathogenesis of hereditary spastic paraplegia (Q28118650) (← links)
- Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation (Q28138281) (← links)
- Hereditary spastic paraplegia caused by mutations in the SPG4 gene (Q28141674) (← links)
- SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia (Q28182779) (← links)
- Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia (Q28201186) (← links)
- Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia (Q28202729) (← links)