Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)-Reference-Cited by-同舟云学术

Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)

Published:2017-08-07 Issue:8 Volume:12 Page:e0181791
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Hayashi Shin^ORCID,Uehara Daniela Tiaki,Tanimoto Kousuke,Mizuno Seiji,Chinen Yasutsugu,Fukumura Shinobu,Takanashi Jun-ichi^ORCID,Osaka Hitoshi,Okamoto Nobuhiko,Inazawa Johji

Funder

Joint Usage/Research Program of Medical Research Institute, Tokyo Medical and Dental University

Japan Society for the Promotion of Science (JP)

Ministry of Education, Culture, Sports, Science and Technology (JP)

Ministry of Health, Labour and Welfare (JP)

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference48 articles.

1. Mapping and expression analysis of the human CASK gene;D Stevenson;Mamm Genome,2000

2. The role of the MAGUK protein CASK in neural development and synaptic function;YP Hsueh;Curr Med Chem,2006