טוען...

Analysis of COQ2 gene in multiple system atrophy

BACKGROUND: Loss of function COQ2 mutations results in primary CoQ10 deficiency. Recently, recessive mutations of the COQ2 gene have been identified in two unrelated Japanese families with multiple system atrophy (MSA). It has also been proposed that specific heterozygous variants in the COQ2 gene m...

תיאור מלא

שמור ב:

מידע ביבליוגרפי
הוצא לאור ב:	Mol Neurodegener
Main Authors:	Ogaki, Kotaro, Fujioka, Shinsuke, Heckman, Michael G, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Labbé, Catherine, Walton, Ronald L, Lorenzo-Betancor, Oswaldo, Wang, Xue, Asmann, Yan, Rademakers, Rosa, Graff-Radford, Neill, Uitti, Ryan, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BioMed Central 2014
נושאים:	Research Article
גישה מקוונת:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4233093/ https://ncbi.nlm.nih.gov/pubmed/25373618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1326-9-44
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

Analysis of COQ2 gene in multiple system atrophy

פריטים דומים