MeSH Browser

MeSH Supplementary: SMCR8 protein, human
Unique ID: C000624213
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000624213
Entry Term(s): Smith-Magenis syndrome chromosome region candidate 8 protein, human
Registry Numbers: 0
Heading Mapped to: *Carrier Proteins
Frequency: 11
Source: Acta Neuropathol Commun. 2016 Apr 27;4(1)51
Date of Entry: 2017/10/23
Revision Date: 2017/10/23

SMCR8 protein, human MeSH Supplementary Concept Data 2025