MeSH Browser

MeSH Supplementary: FGD1 protein, human
Unique ID: C490796
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C490796
Entry Term(s): ZFYVE3 protein, human; faciogenital dysplasia (Aarskog-Scott syndrome) protein, human; faciogenital dysplasia 1 protein, human
Registry Number: 0
Previous Indexing: *PROTEINS (2004-2006)
Heading Mapped to: *Guanine Nucleotide Exchange Factors
Frequency: 69
Note: RefSeq NM_004463
Date of Entry: 2004/09/29
Revision Date: 2006/05/19

FGD1 protein, human MeSH Supplementary Concept Data 2024