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pro vyhledávání: '"Sawsan Ben Romdhane"'
Autor:
Leila Lehkim, François-Jérôme Authier, Sawsan Ben Romdhane, Nouha Farhat, Salma Sakka, Mariem Dammak, Khaireddine Ben Mahfoudh, Yasmine Baba Amer, Sabrine Rekik, Chokri Mhiri
Publikováno v:
Molecular biology reports. 47(8)
Dysferlinopathies belong to the heterogeneous group of autosomal recessive muscular disorders, caused by mutations in the dysferlin gene and characterized by a high degree of clinical variability even though within the same family. This study aims to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76e0e455e98d2a643b2a82e24009f535
https://pubmed.ncbi.nlm.nih.gov/32666437
https://pubmed.ncbi.nlm.nih.gov/32666437
