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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Detalles Bibliográficos
Autores principales: Ashtari, Fereshteh, Saliminejad, Kioomars, Ahani, Ali, Kamali, Koorosh, Pahlevanzadeh, Zhamak, Khorshid, Hamid Reza Khorram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3838770/
https://www.ncbi.nlm.nih.gov/pubmed/24286000

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