Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease-Reference-Cited by-同舟云学术

Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

Published:2010-02-05 Issue:2 Volume:6 Page:e1000833
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Morgan Neil V.,Morris Mark R.,Cangul Hakan,Gleeson Diane,Straatman-Iwanowska Anna,Davies Nicholas,Keenan Stephen,Pasha Shanaz,Rahman Fatimah,Gentle Dean,Vreeswijk Maaike P. G.,Devilee Peter,Knowles Margaret A.,Ceylaner Serdar,Trembath Richard C.,Dalence Carlos,Kismet Erol,Köseoğlu Vedat,Rossbach Hans-Christoph,Gissen Paul,Tannahill David,Maher Eamonn R.

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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5. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.;U Zur Stadt;Hum Mut,2006

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