Association between a novel mutation in SLC20A2 and familial idiopathic basal ganglia calcification.

Familial idiopathic basal ganglia calcification (FIBGC) is a rare, autosomal dominant disorder involving bilateral calcification of the basal ganglia. To identify gene mutations related to a Chinese FIBGC lineage, we evaluated available individuals in the family using CT scans. DNA was extracted fro...

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Autores principales: Yang Zhang, Xianan Guo, Anhua Wu
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/494813e2b3f343a595a5560fbe6bd6ff
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