Open AccessA rare case of COL71A1 heterozygous mutations resulting in neonatal dystrophic epidermolysis bullosa
Author(s) -
Q Q Yuan,
DanNing Hu,
Ting Zhu,
Q.W. Zhang,
Yunhui Gong
Publication year - 2020
Publication title -
clinical and experimental obstetrics and gynecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.157
H-Index - 33
eISSN - 2709-0094
pISSN - 0390-6663
DOI - 10.31083/j.ceog.2020.03.5336
Subject(s) - medicine , epidermolysis bullosa , dermatology , epidermolysis bullosa dystrophica , compound heterozygosity , genetic counseling , prenatal diagnosis , mutation , pediatrics , pregnancy , genetics , fetus , gene , biology
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