MeSH Browser

MeSH Supplementary: CLN3 protein, human
Unique ID: C105199
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C105199
Entry Term(s): Batten disease protein CLN3, human; Batten disease protein, human; battenin protein, human; ceroid lipofuscinosis, neuronal 3 protein, human; ceroid-lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) protein, human
Registry Numbers: 0
Heading Mapped to: *Membrane Glycoproteins; *Molecular Chaperones
Frequency: 237
Note: Defects in CLN3 are the cause of BATTEN DISEASE; also known as juvenile-onset ceroid lipofuscinosis neuronal type 3 (CLN3); RefSeq NM_000086
Source: Genomics 1997 Mar 1;40(2):346-50
Indexing Information: Neuronal Ceroid-Lipofuscinoses
Date of Entry: 1997/04/21
Revision Date: 2006/05/11

CLN3 protein, human MeSH Supplementary Concept Data 2025