Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients by Mabrouk, Imed, Al-Harthi, Nawal, Mani, Rahma, Montantin, Guy, Tissier, Sylvie, Lagha, Rihab, Ben Abdallah, Fethi, Hassan, Mohamad M, Alhomrani, Majid, Gaber, Ahmed, Alsanie, Walaa F, Ouali, Hanadi, Jambi, Fatma A, Almaghamsi, Talal M, Alqarni, Nawal A, Alfarsi, Nawaf A, Kashgari, Khadija, Al-Zahrani, Hasna J, Al-Shamary, Zamel A, Al-Harbi, Abdullah, Amselem, Serge, Escudier, Estelle, Legendre, Marie

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