Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family.

DISCUSSION: We first established the PND procedure with pathogenicity assessment in FXIIID patients. The F13A gene mutations' spectrum of the Chinese Han population was enriched. PMID: 29307277 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/29307277?dopt=Abstract

Source: Hematology - January 10, 2018 Category: Hematology Tags: Hematology Source Type: research