Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype-Reference-Cited by-同舟云学术

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Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Published:2011-01-25 Issue:4 Volume:48 Page:251-255
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Ostergaard P.,Simpson M. A.,Brice G.,Mansour S.,Connell F. C.,Onoufriadis A.,Child A. H.,Hwang J.,Kalidas K.,Mortimer P. S.,Trembath R.,Jeffery S.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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