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CLN3 protein, human MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
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