Complete paternal uniparental isodisomy for chromosome 1 revealed by mutation analyses of the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with congenital insensitivity to pain with anhidrosis.

Source:http://linkedlifedata.com/resource/pubmed/id/11071380

Download in:

View as

General Info

PMID
11071380