학술논문
Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients
Document Type
Article
Author
Mabrouk, I.; Al-Harthi, N.; Lagha, R.; Ben Abdallah, F.; Hassan, M.M.; Gaber, A.; Mani, R.; Amselem, S.; Escudier, E.; Legendre, M.; Montantin, G.; Tissier, S.; Alhomrani, M.; Alsanie, W.F.; Ouali, H.; Jambi, F.A.; Almaghamsi, T.M.; Alqarni, N.A.; Alfarsi, N.A.; Kashgari, K.; Al-Zahrani, H.J.; Al-Shamary, Z.A.; Al-Harbi, A.
Source
In: Journal of Human Genetics . (Journal of Human Genetics, July 2022, 67(7):381-386)
Subject
Language
English
ISSN
1435232X
14345161
14345161