Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fangqi, He"'
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Hypohidrotic ectodermal dysplasia (HED) is a common recessive X-linked hereditary disease that affects the development of ectoderm. Gene mutations of ectodysplasin A (EDA) play key roles in process of this disease. In our prelimin
Externí odkaz:
https://doaj.org/article/4eddb4418106429da3f0eeeaf1bc87eb
Autor:
Fangqi He
Publikováno v:
INTERNATIONAL JOURNAL OF HUMAN GENETICS. 22
To investigate the protein expression changes of c.878T>G mutant and wild-type Ectodysplasin-A (EDA) gene on prokaryotic vectors from hypohidrotic ectodermal dysplasia (HED) families. The c.878T>G mutant and wild-type EDA genes were amplified, screen
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 43(7)
To analyze the incidence and distribution of oral mucosal diseases in Hunan Province and provide reference for prevention and treatment. Methods: The clinical data for all patients, who were treated in Xiangya Hospital of Central South University fro