Pages that link to "Q59700957"
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The following pages link to Patrick A Dion (Q59700957):
Displaying 50 items.
- Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease (Q22242985) (← links)
- C9orf72 repeat expansions are a rare genetic cause of parkinsonism (Q23936600) (← links)
- VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families (Q24298278) (← links)
- Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia (Q24317205) (← links)
- ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19 (Q24600461) (← links)
- Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia (Q24680886) (← links)
- Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice (Q28238845) (← links)
- NEK1 variants confer susceptibility to amyotrophic lateral sclerosis (Q28277378) (← links)
- Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families (Q28302988) (← links)
- LINGO1 variants in the French-Canadian population (Q28743588) (← links)
- Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics (Q30009842) (← links)
- Where are the missing pieces of the schizophrenia genetics puzzle? (Q33350546) (← links)
- Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis (Q33564738) (← links)
- A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors (Q34114542) (← links)
- WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio) (Q34539896) (← links)
- Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissues (Q34603854) (← links)
- Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis (Q35063153) (← links)
- Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans (Q35070967) (← links)
- KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2. (Q35161567) (← links)
- Early detection of structural abnormalities and cytoplasmic accumulation of TDP-43 in tissue-engineered skins derived from ALS patients (Q35176790) (← links)
- Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways (Q35624305) (← links)
- Genetic markers of Restless Legs Syndrome in Parkinson disease (Q35638885) (← links)
- Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population (Q35641758) (← links)
- Mutation burden of rare variants in schizophrenia candidate genes (Q35651460) (← links)
- Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. (Q35906336) (← links)
- Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum (Q36003995) (← links)
- GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder (Q36072435) (← links)
- Exome sequencing identifies FUS mutations as a cause of essential tremor (Q36152927) (← links)
- Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals (Q36159225) (← links)
- Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD (Q36616570) (← links)
- Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the disease (Q36689017) (← links)
- CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia (Q36809438) (← links)
- Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia (Q36891484) (← links)
- De novo variants in sporadic cases of childhood onset schizophrenia (Q36902721) (← links)
- The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder (Q36968317) (← links)
- Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia (Q37010397) (← links)
- Analysis of the effects of rare variants on splicing identifies alterations in GABAA receptor genes in autism spectrum disorder individuals (Q37044353) (← links)
- Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum (Q37058033) (← links)
- GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis (Q37245142) (← links)
- Recent advances in the genetics of amyotrophic lateral sclerosis (Q37434642) (← links)
- Genetics of motor neuron disorders: new insights into pathogenic mechanisms (Q37613452) (← links)
- Genome-wide association study in essential tremor identifies three new loci (Q37739868) (← links)
- Schizophrenia genetics: putting all the pieces together (Q37997954) (← links)
- Molecular aspects of hereditary spastic paraplegia (Q38196130) (← links)
- Dissection of genetic factors associated with amyotrophic lateral sclerosis (Q38208161) (← links)
- Genetics of essential tremor: from phenotype to genes, insights from both human and mouse studies (Q38211291) (← links)
- Amyotrophic lateral sclerosis: new genes, new models, and new mechanisms (Q38363759) (← links)
- FOXP1-related intellectual disability syndrome: a recognisable entity (Q38666337) (← links)
- CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders (Q38727086) (← links)
- ALS: Recent Developments from Genetics Studies (Q38817325) (← links)