Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sajad Sheikh-kanlomilan"'
Autor:
Milad Ebrahimi, Mahdieh Behnam, Nafiseh Behranvand-jazi, Ladan Yari, Sajad Sheikh-kanlomilan, Mansoor Salehi, Pardis Tahmasebi, Mohaddeseh Amini, Mohaddeseh Behjati, Nafisehsadat Hosseini
Publikováno v:
Journal of Research in Medical Sciences, Vol 22, Iss 1, Pp 100-100 (2017)
Background: Mutations in the acid alpha-glucosidase (GAA) gene usually lead to reduced GAA activity. In this study, we analyzed the mutations of GAA and GAA enzyme activity from one sibling suspected Pompe disease and their first-degree relatives. Ma
Externí odkaz:
https://doaj.org/article/048e8a4764ae4f92a408354a19d11f39
Autor:
Sajad Sheikh-Kanlomilan, Nafiseh Behranvand-Jazi, Nafisehsadat Hosseini, Mohaddeseh Behjati, Ladan Yari, Milad Ebrahimi, Mansoor Salehi, Mohaddeseh Amini, Pardis Tahmasebi, Mahdieh Behnam
Publikováno v:
Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences
Journal of Research in Medical Sciences, Vol 22, Iss 1, Pp 100-100 (2017)
Journal of Research in Medical Sciences, Vol 22, Iss 1, Pp 100-100 (2017)
Background: Mutations in the acid alpha-glucosidase (GAA) gene usually lead to reduced GAA activity. In this study, we analyzed the mutations of GAA and GAA enzyme activity from one sibling suspected Pompe disease and their first-degree relatives. Ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59586d66af9225e2f5258677525d9250
http://europepmc.org/articles/PMC5583621
http://europepmc.org/articles/PMC5583621