Title : Genomic organization of the human NTRK1 gene.

Pub. Date : 1996 Dec 5

PMID : 8957089






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 RET is affected by germ line and somatic mutations in MEN2A, MEN2B tumor syndromes and in the abnormal developmental Hirschsprung disease, whereas mutations of NTRK1 have been reported very recently in patients with congenital insensitivity to pain with anidrosis (CIPA). 3-(2-carboxyindol-3-yl)propionic acid ret proto-oncogene Homo sapiens