Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mohamed Soliman Elsheikh"'
Autor:
Bibi Zainab, Zainab Ayaz, Anum Munir, Ahmed Hossam Mahmoud, Mohamed Soliman Elsheikh, Azhar Mehmood, Sajid Khan, Muhammad Rizwan, Kainat Jahangir, Arshad Mehmood Abbasi
Publikováno v:
Journal of King Saud University: Science, Vol 32, Iss 3, Pp 1793-1811 (2020)
Achromatopsia (ACHM) is a genetically heterogeneous visual disorder, also known as rod monochromatism, in which human get affected due to cone cells. Mutation in five genes viz. CNGA3, CNGB3, GNAT2, PDE6C, and PDE6H have been reported in ACHM. These
Externí odkaz:
https://doaj.org/article/e983407568ba4d3c85b5ca0d085f01e5
Autor:
Zainab Ayaz, Muhammad Rizwan, Anum Munir, Azhar Mehmood, Ahmed Hossam Mahmoud, Mohamed Soliman Elsheikh, Bibi Zainab, Kainat Jahangir, Sajid Khan, Arshad Mehmood Abbasi
Publikováno v:
Journal of King Saud University: Science, Vol 32, Iss 3, Pp 1793-1811 (2020)
Achromatopsia (ACHM) is a genetically heterogeneous visual disorder, also known as rod monochromatism, in which human get affected due to cone cells. Mutation in five genes viz. CNGA3, CNGB3, GNAT2, PDE6C, and PDE6H have been reported in ACHM. These
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c724c282d4157fb7d25a011770ed094c
http://www.sciencedirect.com/science/article/pii/S1018364720300239
http://www.sciencedirect.com/science/article/pii/S1018364720300239