MeSH Browser

MeSH Supplementary: CLN8 protein, human
Unique ID: C121767
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C121767
Entry Term(s): EPMR protein, human; ceroid-lipofuscinosis, neuronal 8 protein, human; epilepsy, progressive with mental retardation protein, human
Registry Numbers: 0
Heading Mapped to: *Membrane Proteins
Frequency: 40
Note: RefSeq NM_018941
Source: Nat Genet 1999 Oct;23(2):233-6
Date of Entry: 1999/10/27
Revision Date: 2006/05/11

CLN8 protein, human MeSH Supplementary Concept Data 2025