المؤلفون: 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

المصدر: Journal of Human Genetics. 67:381-386

مصطلحات موضوعية: Cytoskeletal Proteins, Kartagener Syndrome, Mutation, Saudi Arabia, Genetics, High-Throughput Nucleotide Sequencing, Humans, Founder Effect, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d759d8adafe10b5b6a4b47a39483c1f
https://doi.org/10.1038/s10038-021-01006-9