Zobrazeno 1 - 1
of 1
pro vyhledávání: '"agenesis of left pulmonary artery"'
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 4, Iss 2, Pp 122-125 (2021)
Background: ATP6V1B2 gene mutation is associated with Zimmermann-Laband syndrome 2 (ZLS2), which is a rare developmental disorder characterized by nail hypoplasia and hereditary deafness. Case Presentation: We report a new phenotypic mutation of ATP6
Externí odkaz:
https://doaj.org/article/b47b3da300274a50a5b1bcecdaab648c
