Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability-Reference-Cited by-同舟云学术

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

Published:2012-05 Issue:5 Volume:90 Page:847-855
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Abbasi-Moheb Lia,Mertel Sara,Gonsior Melanie,Nouri-Vahid Leyla,Kahrizi Kimia,Cirak Sebahattin,Wieczorek Dagmar,Motazacker M. Mahdi,Esmaeeli-Nieh Sahar,Cremer Kirsten,Weißmann Robert,Tzschach Andreas,Garshasbi Masoud,Abedini Seyedeh S.,Najmabadi Hossein,Ropers H. Hilger,Sigrist Stephan J.,Kuss Andreas W.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference43 articles.

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2. Genetics of intellectual disability;Ropers;Curr. Opin. Genet. Dev.,2008

3. Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci;Najmabadi;Hum. Genet.,2007

4. Autosomal recessive mental retardation: Homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots;Kuss;Hum. Genet.,2011

5. Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome;Moheb;Eur. J. Hum. Genet.,2008

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