Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification

BACKGROUND: Familial Idiopathic Basal Ganglia Calcification (IBGC) is a rare neurodegenerative disorder which is usually transmitted as an autosomal dominant trait. IBGC is genetically heterogeneous and SLC20A2, on chromosome 8p21.1–8q11.23, is the first gene found in IBGC-affected patients with var...

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Main Authors: Ashtari, Fereshteh, Saliminejad, Kioomars, Ahani, Ali, Kamali, Koorosh, Pahlevanzadeh, Zhamak, Khorshid, Hamid Reza Khorram
格式: Artigo
語言:Inglês
出版: Avicenna Research Institute 2013
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Original Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3838770/
https://ncbi.nlm.nih.gov/pubmed/24286000
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