Article ID Journal Published Year Pages File Type
10143488 Gene 2018 7 Pages PDF
Abstract
Our research expanded the spectrum of the NTRK1 mutations associated with CIPA patients, provided additional clues relating to the phenotype-genotype relationship in CIPA, and summarized the features of the genetic epidemiology of CIPA in the Chinese ethnic group.
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Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Genetics
Preview
Identification of a novel mutation of the NTRK1 gene in patients with congenital insensitivity to pain with anhidrosis (CIPA)
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