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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Detalles Bibliográficos
Autores principales: Zhang, Yang, Guo, Xianan, Wu, Anhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577762/
https://www.ncbi.nlm.nih.gov/pubmed/23437308
http://dx.doi.org/10.1371/journal.pone.0057060

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577762/
https://www.ncbi.nlm.nih.gov/pubmed/23437308
http://dx.doi.org/10.1371/journal.pone.0057060

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