학술논문
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta
Document Type
Journal
Author
Hany, Ummey; Watson, Christopher M.; Liu, Lu; Smith, Claire E. L.; Harfoush, Asmaa; Poulter, James A.; Nikolopoulos, Georgios; Balmer, Richard; Brown, Catriona J.; Patel, Anesha; Simmonds, Jenny; Charlton, Ruth; Acosta de Camargo, Maria Gabriela; Rodd, Helen D.; Jafri, Hussain; Antanaviciute, Agne; Moffat, Michelle; Al-Jawad, Maisoon; Inglehearn, Chris F.; Mighell, Alan J.
Source
Subject
Language
English
ISSN
14686244