Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death

Release time:2017-10-28

Impact Factor:4.486

Journal:J Cell Mol Med

Co-author:Xiang R, Jin J Y, Li J J, Guo S, Fan L L, Chen Y Q, Huang H

Indexed by:Unit Twenty Basic Research

Document Code:10.1111/jcmm.13409

Discipline:生物学

Document Type:J

Volume:22

Issue:2

Page Number:1350-1354

ISSN No.:1582-4934

Translation or Not:no

Date of Publication:2018-01-25

Included Journals:SCI

Links to published journals:http://onlinelibrary.wiley.com/doi/10.1111/jcmm.13409/full