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pro vyhledávání: '"Mohammad Sadegh Nadimifar"'
Autor:
Hossein Aghamollaei, Farhad Nejat, Seyed Aliasghar Mosavi, Saeed Morovvati, Khosrow Jadidi, Mohammad Sadegh Nadimifar
Publikováno v:
Guoji Yanke Zazhi, Vol 17, Iss 6, Pp 1023-1027 (2017)
AIM: To evaluate association between mutations in the visual system homeobox 1(VSX1)gene and keratoconus(KCN)complicated with granular corneal dystrophy(GCD), direct sequencing was performed in an Iranian family affected by KCN and GCD in four genera
Externí odkaz:
https://doaj.org/article/14a1f431a3074a32bec667817c2abfb7