Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice-Reference-Cited by-同舟云学术

Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice

Published:2014-02 Issue:2 Volume:386 Page:395-407
ISSN:0012-1606
Container-title:Developmental Biology
language:en
Short-container-title:Developmental Biology

Author:

Balemans Monique C.M.,Ansar Muhammad,Oudakker Astrid R.,van Caam Arjan P.M.,Bakker Brenda,Vitters Elly L.,van der Kraan Peter M.,de Bruijn Diederik R.H.,Janssen Sanne M.,Kuipers Arthur J.,Huibers Manon M.H.,Maliepaard Eliza M.,Walboomers X. Frank,Benevento Marco,Nadif Kasri Nael,Kleefstra Tjitske,Zhou Huiqing,Van der Zee Catharina E.E.M.,van Bokhoven Hans

Funder

GENCODYS

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,Molecular Biology

Reference52 articles.

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