Preferred Label : Lgi1 protein, mouse;
MeSH note : Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features;
60 kD with 3.5 leucine-rich repeats with conserved flanking sequences; RefSeq NM_020278;
MeSH synonym : leucine-rich repeat LGI family, member 1 protein, mouse;
Is substance : O;
Origin ID : C492120;
UMLS CUI : C1452685;
MeSH term(s) associated for indexing
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