- L1CAM
- L1CAM Mutation Database
Medical dictionary. 2011.
Medical dictionary. 2011.
L1CAM — • L1CAM Mutation Database … Dictionary of medical acronyms & abbreviations
L1 (protein) — L1, also known as L1CAM, is a transmembrane protein; it is a neuronal cell adhesion molecule, member of the L1 protein family, of 200 220 kDa, and involved in axon guidance and cell migration with a strong implication in treatment resistant… … Wikipedia
Neurales Zelladhäsionsmolekül L1 — Zelladhäsionsmolekül L1 Masse/Länge Primärstruktur 1257 aa … Deutsch Wikipedia
Syndrome L1 — Le syndrome L1 regroupe les manifestations liées à la mutation du gène L1CAM Il est caractérisé par l’association des traits suivants : Hydrocéphalie ; Retard mental ; Tonicité augmentée des muscles des jambes (spasticité) ;… … Wikipédia en Français
MASA syndrome — Classification and external resources OMIM 303350 MASA syndrome, also called CRASH syndrome and Gareis Mason syndrome,[1] is a rare X linked recessive[2 … Wikipedia
L1 family — The L1 family is a family of cell adhesion molecules that includes four different L1 like proteins. They are members of the immunoglobulin superfamily (IgSF CAMs). The members of the L1 family in humans are called L1 or L1cam, CHL1 (close… … Wikipedia
CHL1 — protein Name=cell adhesion molecule with homology to L1CAM (close homolog of L1) caption= width= HGNCid=1939 Symbol=CHL1 AltSymbols= EntrezGene=10752 OMIM=607416 RefSeq=NM 006614 UniProt=O00533 PDB= ECnumber= Chromosome=3 Arm=p Band=26… … Wikipedia
OPN1LW — Opsin 1 (cone pigments), long wave sensitive Identifiers Symbols OPN1LW; CBBM; CBP; COD5; RCP; ROP External IDs … Wikipedia
NFASC — Neurofascin Rendering based on PDB 3P3Y … Wikipedia
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