Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients

Sequence variants in SLC41A1 (solute carrier family 41 member 1) within the PARK16 locus have been reported to be associated with Parkinson's disease (PD). We performed direct DNA sequencing of the SLC41A1 gene in 100 early‐onset PD cases. A novel intron variant (NM_173854.5:c.993‐90delA) and a...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part B, Neuropsychiatric genetics Neuropsychiatric genetics, 2015-12, Vol.168B (8), p.706-711
Hauptverfasser:	Wang, Ling, Cheng, Lan, Li, Nan-Nan, Yu, Wen-Juan, Sun, Xiao-Yi, Peng, Rong
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Age of Onset Alleles Asian Continental Ancestry Group - genetics Case-Control Studies Cation Transport Proteins - genetics China - epidemiology Female Genetic Predisposition to Disease Genetics Genome-Wide Association Study Humans Introns Male Middle Aged Parkinson Disease - epidemiology Parkinson Disease - genetics Parkinson's disease Polymorphism, Single Nucleotide rs11240569 Sequence Analysis, DNA SLC41A1 variations
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!