Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations-Reference-Cited by-同舟云学术

Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations

Published:2019-10 Issue: Volume:293 Page:186-191
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Gao Linggen,Tian Tao,Zhou Xianliang,Fan Li,Wang Rong,Wu Haiying

Funder

Military Healthcare Fund

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference50 articles.

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