학술논문
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals
Document Type
Article
Author
Sczakiel, H.L.; Zhao, M.; Danyel, M.; Ehmke, N.; Seelow, D.; Horn, D.; Boschann, F.; Wollert-Wulf, B.; Janz, M.; Stoltenburg, C.; Damseh, N.; Al-Ashhab, M.; Balci, T.B.; Osmond, M.; Andrade, A.; Schallner, J.; Porrmann, J.; McDonald, K.; Liao, M.; Oppermann, H.; Platzer, K.; Dierksen, N.; Mojarrad, M.; Eslahi, A.; Bakaeean, B.; Calame, D.G.; Lupski, J.R.; Firoozfar, Z.; Seyedhassani, S.M.; Mohammadi, S.A.; Anwaar, N.; Rahman, F.; Maroofian, R.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, August 2023, 31(8):905-917)
Subject
Language
English
ISSN
14765438
10184813
10184813