De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability-Reference-Cited by-同舟云学术

De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability

Published:2014-04 Issue:4 Volume:94 Page:618-624
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Grozeva Detelina,Carss Keren,Spasic-Boskovic Olivera,Parker Michael J.,Archer Hayley,Firth Helen V.,Park Soo-Mi,Canham Natalie,Holder Susan E.,Wilson Meredith,Hackett Anna,Field Michael,Floyd James A.B.,Hurles Matthew,Raymond F. Lucy

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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