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Objective: Congenital myopathy as a nosologic entity has long been recognized, but knowledge of overall and subtype prevalence and phenotype-genotype relationship is scarce, especially in the adult po...
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Objective: To assess the contribution of variants in STK32B , PPARGC1A , and CTNNA3 as essential tremor (ET) predisposing factors following their association in a 2-stage genome-wide association study...
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Neurology Genetics | A peer-reviewed clinical and translational neurology open access journal
Notable This Week RESEARCH ARTICLE | Neuromuscular Disease
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Web host: | CloudFlare, Inc. |
Registrar: | Public Interest Registry |
Registrant: | American Academy of Neurology |
Updated: | November 21, 2023 |
Expires: | June 13, 2032 |
Created: | June 14, 1996 |
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