Rahma Mani

Years Active: 2019-2022
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Imed Mabrouk, Nawal Al-Harthi, Rahma Mani, Guy Montantin, Sylvie Tissier, Rihab Lagha, Fethi Ben Abdallah, Mohamad M Hassan, Majid Alhomrani, Ahmed Gaber, Walaa F Alsanie, Hanadi Ouali, Fatma A Jambi, Talal M Almaghamsi, Nawal A Alqarni, Nawaf A Alfarsi, Khadija Kashgari, Hasna J Al-Zahrani, Zamel A Al-Shamary, Abdullah Al-Harbi, Serge Amselem, Estelle Escudier, Marie Legendre
Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients. Journal of human genetics 67 (7) (2022)
Rahma Mani, Sabrina Belkacem, Zohra Soua, Sandra Chantot, Guy Montantin, Sylvie Tissier, Bruno Copin, Jihene Bouguila, Nicolas Rive Le Gouard, Lamia Boughamoura, Salma Ben Ameur, Mongia Hachicha, Raoudha Boussoffara, Khadija Boussetta, Samia Hammouda, Abir Bedoui, Habib Besbes, Seif Meddeb, Karima Chraeit, Monia Khlifa, Estelle Escudier, Serge Amselem, Imed Mabrouk, Marie Legendre
Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele. Human mutation 41 (1) (2019)

Rahma Mani.css-eqlu8i{font-size:small;padding-left:4px;}