MeSH Browser

MeSH Supplementary: EPS8L3 protein, human
Unique ID: C581607
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C581607
Entry Term(s): EPS8-like 3 protein, human
Registry Numbers: 0
Heading Mapped to: *Adaptor Proteins, Signal Transducing
Frequency: 6
Note: EPS8L3 is a causative gene for Marie Unna hereditary hypotrichosis; RefSeq NM_024526
Source: J Med Genet. 2012 Dec;49(12):727-30
Date of Entry: 2013/06/12
Revision Date: 2013/06/12

EPS8L3 protein, human MeSH Supplementary Concept Data 2025