NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes
Ayaz Khan(National Institute for Biotechnology and Genetic Engineering), Chunyu Liu(Jiamusi University), Humayoon Shafique Satti(National University of Medical Sciences), Raees Khan(National University of Medical Sciences), Muhammad Safeer(Hazara University), Julien Fauré(Centre Hospitalier Universitaire de Grenoble), Ilyas Ahmad(Kohat University of Science and Technology), Naveed Altaf Malik(National Institute for Biotechnology and Genetic Engineering), Sheraz Khan(Ahvaz Jundishapur University of Medical Sciences), Xénia Latypova, Shixiong Tian(Geological Exploration Technology Institute of Jiangsu Province), Shahid Mahmood Baig(National Institute for Biotechnology and Genetic Engineering), John Rendu(Centre Hospitalier Universitaire de Grenoble), Tahir Naeem Khan(National University of Medical Sciences), Naimat Ullah(National Institute for Biotechnology and Genetic Engineering), Nazia Akbar(Hazara University), Iram Javed, Feng Zhang(Affiliated Hospital of North Sichuan Medical College), Muhammad Tariq(Jiangsu University), Mahnoor Asif(National Institute for Biotechnology and Genetic Engineering), Muhammad Naeem(Quaid-i-Azam University), Mahwish Ali(National University of Medical Sciences), Shahid Ullah(University of Peshawar)
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