Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability-Reference-Cited by-同舟云学术

Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability

Published:2014-03-13 Issue:15 Volume:23 Page:4015-4023
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bernkopf Marie,Webersinke Gerald,Tongsook Chanakan,Koyani Chintan N.,Rafiq Muhammad A.,Ayaz Muhammad,Müller Doris,Enzinger Christian,Aslam Muhammad,Naeem Farooq,Schmidt Kurt,Gruber Karl,Speicher Michael R.,Malle Ernst,Macheroux Peter,Ayub Muhammad,Vincent John B.,Windpassinger Christian,Duba Hans-Christoph

Publisher

Oxford University Press (OUP)

Subject

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

Reference23 articles.

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2. The genetic basis of non-syndromic intellectual disability: a review;J. Neurodev. Disord.,2010

3. Genetics of recessive cognitive disorders;Trends Genet.,2014

4. Mutation in NSUN2, which encodes an RNA methlytransferase, causes autosomal-recessive intellectual disability;Am. J. Hum. Genet.,2012

5. Mutations in NSUN2 cause autosomal-recessive intellectual disability;Am. J. Hum. Genet.,2012

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