Rapid diagnostic testing of a neonate in a family with hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy (HCM) is a common but severe genetic disease. A pregnant woman with familial HCM was referred to our hospital as both the couple and their families were concerned that the baby would later develop HCM. Therefore, we determined the risk of HCM in the neonate. Usin...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: H. Ueda, T. Miyamoto, Y. Tsurusaki, G. Minase, N. Matsumoto, K. Sengoku
Format: Artigo
Sprog:Inglês
Udgivet: IMR Press 2020-08-01
Serier:Clinical and Experimental Obstetrics & Gynecology
Fag:
early diagnosis
hypertrophic cardiomyopathy
mutation
myh7
whole-exome sequencing
Online adgang:https://www.imrpress.com/journal/CEOG/47/4/10.31083/j.ceog.2020.04.3433
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker