Mutations in the histamineN-methyltransferase gene,HNMT, are associated with nonsyndromic autosomal recessive intellectual disability-Reference-Cited by-同舟云学术

Mutations in the histamineN-methyltransferase gene,HNMT, are associated with nonsyndromic autosomal recessive intellectual disability

Published:2015-07-23 Issue:20 Volume:24 Page:5697-5710
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Heidari Abolfazl,Tongsook Chanakan,Najafipour Reza,Musante Luciana,Vasli Nasim,Garshasbi Masoud,Hu Hao,Mittal Kirti,McNaughton Amy J. M.,Sritharan Kumudesh,Hudson Melissa,Stehr Henning,Talebi Saeid,Moradi Mohammad,Darvish Hossein,Arshad Rafiq Muhammad,Mozhdehipanah Hossein,Rashidinejad Ali,Samiei Shahram,Ghadami Mohsen,Windpassinger Christian,Gillessen-Kaesbach Gabriele,Tzschach Andreas,Ahmed Iltaf,Mikhailov Anna,Stavropoulos D. James,Carter Melissa T.,Keshavarz Soraya,Ayub Muhammad,Najmabadi Hossein,Liu Xudong,Ropers Hans Hilger,Macheroux Peter,Vincent John B.

Funder

Canadian Institutes of Health Research

Max Planck Society

GENCODYS

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/20/5697/13926674/ddv286.pdf

Reference44 articles.

1. Prevalence of intellectual disability: A meta-analysis of population-based studies