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Identification of two novel compound heterozygous CLCN1 mutations associated with autosomal recessive myotonia congenita.
Neurol Res. 2019 Dec;41(12):1069-1074. doi: 10.1080/01616412.2019.1672392. Epub 2019 Sep 30.
Neurol Res. 2019.
PMID: 31566103
Parkinson's Disease and Homocysteine: A Community-Based Study in a Folate and Vitamin B12 Deficient Population.
Wei Z, Tiandong W, Yang L, Huaxing M, Guowen M, Yalan F, Xiaoyuan N.
Wei Z, et al. Among authors: huaxing m.
Parkinsons Dis. 2016;2016:9539836. doi: 10.1155/2016/9539836. Epub 2016 Aug 31.
Parkinsons Dis. 2016.
PMID: 27656311
Free PMC article.
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