Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation-Reference-Cited by-同舟云学术

Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation

Published:2012-03-03 Issue:4 Volume:87 Page:377-383
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Zhang Clarence K.,Stein Philip B.,Liu Jun,Wang Zuoheng,Yang Ruhua,Cho Judy H.,Gregersen Peter K.,Aerts Johannes M.F.G.,Zhao Hongyu,Pastores Gregory M.,Mistry Pramod K.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23118/fullpdf

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