MeSH Browser

MeSH Supplementary: NIPA1 protein, human
Unique ID: C478824
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C478824
Entry Term(s): SPG6 protein, human; non imprinted in Prader-Willi-Angelman syndrome 1 protein, human; spastic paraplegia 6 (autosomal dominant) protein, human
Registry Numbers: 0
Heading Mapped to: *Membrane Proteins
Frequency: 45
Note: RefSeq NM_144599
Source: Am J Hum Genet 2003 Oct;73(4):898-925
Date of Entry: 2003/11/18
Revision Date: 2006/06/23

NIPA1 protein, human MeSH Supplementary Concept Data 2025