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pro vyhledávání: '"Clara-Sophie Kossel"'
Autor:
Clara-Sophie Kossel, Mandy Wahlbuhl, Sonia Schuepbach-Mallepell, Jung Park, Christine Kowalczyk-Quintas, Michaela Seeling, Klaus von der Mark, Pascal Schneider, Holm Schneider
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
X-linked hypohidrotic ectodermal dysplasia with the cardinal symptoms hypodontia, hypotrichosis and hypohidrosis is caused by a genetic deficiency of ectodysplasin A1 (EDA1). Prenatal EDA1 replacement can rescue the development of skin appendages and
Externí odkaz:
https://doaj.org/article/29f8c79279b345aaa0a27af1af43f8d9