Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Marzieh Mohammadi Anaie"'
Autor:
Siavash Shakerian, Gholamreza Shariati, Marzieh Mohammadi anaie, Nehzat Abdorasouli, Fatemeh Nanvazadeh, Hamid Galehdari, Mohammad Hamid, Alireza Sedaghat, Alihossein Saberi
Background:Spinal muscular atrophy (SMA) is a rare autosomal recessive inherited neuromuscular disease with about 1:6000 to 1:10,000 in newborns. Objectives:To evaluate the copy number variation of SMN1 and SMN2 genes between two generations, we expe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b72afee84bfe1c8478bd7774b2d2eee
https://doi.org/10.21203/rs.3.rs-2029090/v1
https://doi.org/10.21203/rs.3.rs-2029090/v1
Autor:
Alireza Sedaghat, Alihossein Saberi, Siavash Shakerian, Marzieh Mohammadi Anaie, Mostafa Sedighi, Fateme Nanvazadeh, Nehzat Abdorasouli, Gholamreza Shariati
Publikováno v:
Meta Gene. 23:100641
Background Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked disorders caused by the mutation within the dystrophin gene. Objectives the primary objective of this study was to evaluate the deletion and duplication mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1e8dfc3fd6fb489c4ec4ba6db79dcc4
https://doi.org/10.1016/j.mgene.2019.100641
https://doi.org/10.1016/j.mgene.2019.100641
