Chromodomain proteins in development: lessons from CHARGE syndrome

Layman WS, Hurd EA, Martin DM. Chromodomain proteins in development: lessons from CHARGE syndrome. In humans, heterozygous mutations in the adenosine triphosphate‐dependent chromatin remodeling gene CHD7 cause CHARGE syndrome, a common cause of deaf–blindness, balance disorders, congenital heart mal...

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Veröffentlicht in:	Clinical genetics 2010-07, Vol.78 (1), p.11-20
Hauptverfasser:	Layman, WS, Hurd, EA, Martin, DM
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple Animals Biological and medical sciences Birth defects CHARGE syndrome CHD7 chromodomain helicase DNA-binding gene 7 Deaf-Blind Disorders - physiopathology Development DNA Helicases - deficiency DNA Helicases - physiology DNA-Binding Proteins - deficiency DNA-Binding Proteins - physiology Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling Genetic disorders Genetics of eukaryotes. Biological and molecular evolution Genotype & phenotype Growth and Development Humans Medical genetics Medical sciences Mice Molecular and cellular biology Mutation Rodents Syndrome
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