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<i>TMEM230</i> is not a gene for Parkinson’s diseaseDOI 10.1101/097030
Reanalysis of genetic variants detected by next generation sequencing in Parkinson’s disease with two novel variantsSemantic proximity
Genetic causes of Parkinson?s disease: UCHL-1Semantic proximity
Noncompaction and the novel variant c.425A>T in TPM1.Semantic proximity
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian populationSemantic proximity
Exome‐Wide Analyses in Paroxysmal Kinesigenic Dyskinesia Confirm <scp> <i>TMEM151A</i> </scp> as a Novel Causative GeneSemantic proximity
Controversy of TMEM230 Associated with Parkinson's Disease.Semantic proximity
Dynamic mutations: a new class of mutations causing human disease.Semantic proximity
Gene table of monogenic neuromuscular disorders (nuclear genome only) Vol. 18 No. 1, January 2008.Semantic proximity
RHD Tyr311Stop encoded by a novel nonsense mutation.Semantic proximity
Identification of TMEM230 mutations in familial Parkinson’s disease (response to comments)Semantic proximity
Novel human pathological mutations.Semantic proximity
TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?Semantic proximity
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