A novel nonsense GPSM2 mutation in a Yemeni family underlying Chudley-McCullough syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference17 articles.
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2. Chudley-McCullough syndrome: another report and a brief review of the literature;Alrashdi;Clin. Dysmorphol.,2011
3. Comprehensive analysis of deafness genes in families with autosomal recessive nonsyndromic hearing loss;Atik;PloS One,2015
4. Expression analysis and subcellular distribution of the two G-protein regulators AGS3 and LGN indicate distinct functionality. Localization of LGN to the midbody during cytokinesis;Blumer;J. Biol. Chem.,2002
5. Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder;Chudley;Am. J. Med. Genet.,1997
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