EXOME SEQUENCING IDENTIFIES A NOVEL TRPV4 MUTATION IN A CMT2C FAMILY

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Neurology 2012-07, Vol.79 (2), p.192-194
Hauptverfasser:	LANDOURE, Guida, SULLIVAN, Jeremy M, TRAYNOR, Bryan J, BURNETT, Barrington G, SUMNER, Charlotte J, JOHNSON, Janel O, MUNNS, Clare H, YIJUN SHI, DIALLO, Oumarou, RAPHAEL GIBBS, J, GAUDET, Rachelle, LUDLOW, Christy L, FISCHBECK, Kenneth H
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Charcot-Marie-Tooth Disease - genetics Clinical/Scientific Notes Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Exome - genetics Humans Medical sciences Mutation - genetics Neurology Pedigree TRPV Cation Channels - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!