ALS2 protein, human

Preferred Label : ALS2 protein, human;

MeSH note : mutated in a form of amyotrophic lateral sclerosis; Defects in ALS2 are the cause of AMYOTROPHIC LATERAL SCLEROSIS (ALS); RefSeq NM_020919;

MeSH synonym : amyotrophic lateral sclerosis 2 (juvenile) protein, human; alsin, human;

Is substance : O;

Détails

Origin ID

C438187;

UMLS CUI

C1098466;

MeSH indexing information
- amyotrophic lateral sclerosis [MeSH Descriptor]
MeSH term(s) associated for indexing
- guanine nucleotide exchange factors [MeSH Descriptor]
Record concept(s)
- ALS2 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients