MeSH Browser

MeSH Supplementary: CHD7 protein, human
Unique ID: C491434
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C491434
Entry Term(s): CHD7S protein, human; chromodomain helicase DNA binding protein 7, human
Registry Number: EC 3.6.4.12
Heading Mapped to: *DNA Helicases; *DNA-Binding Proteins
Frequency: 247
Note: RefSeq XM_098762
Source: Nat Genet 2004 Sep;36(9):955-7
Indexing Information: Kallmann Syndrome; Protein Isoforms; CHARGE Syndrome
Date of Entry: 2004/10/03
Revision Date: 2013/02/08

CHD7 protein, human MeSH Supplementary Concept Data 2024