Items where Author is "Ansar, Muhammad"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type | Refereed
Jump to: 2022 | 2020 | 2015
Number of items: 4.


Ansar, Muhammad and Javed, Samra and Baig, Hafiz Muhammad Azhar and Quinodoz, Mathieu and Ullah, Mukhtar and Han, Ji Hoon and Rahim, Muhammad Usama and Kausar, Humera and Calzetti, Giacomo and Rivolta, Carlo. (2022) A new nonsense mutation in; HMX1; in two siblings with oculoauricular syndrome. Ophthalmic Genetics, 43 (5). pp. 720-723.


Poulter, James A. and Gravett, Molly S. C. and Taylor, Rachel L. and Fujinami, Kaoru and De Zaeytijd, Julie and Bellingham, James and Rehman, Atta Ur and Hayashi, Takaaki and Kondo, Mineo and Rehman, Abdur and Ansar, Muhammad and Donnelly, Dan and Toomes, Carmel and Ali, Manir and U. K. Inherited Retinal Disease Consortium, and De Baere, Elfride and Leroy, Bart P. and Davies, Nigel P. and Henderson, Robert H. and Webster, Andrew R. and Rivolta, Carlo and Mahroo, Omar A. and Arno, Gavin and Black, Graeme C. M. and McKibbin, Martin and Harris, Sarah A. and Khan, Kamron N. and Inglehearn, Chris F.. (2020) New variants and in silico analyses in GRK1 associated Oguchi disease. Human Mutation. pp. 1-13.

Ansar, Muhammad and Ranza, Emmanuelle and Shetty, Madhur and Paracha, Sohail A. and Azam, Maleeha and Kern, Ilse and Iwaszkiewicz, Justyna and Farooq, Omer and Pournaras, Constantin J. and Malcles, Ariane and Kecik, Mateusz and Rivolta, Carlo and Muzaffar, Waqar and Qurban, Aziz and Ali, Liaqat and Aggoun, Yacine and Santoni, Federico A. and Makrythanasis, Periklis and Ahmed, Jawad and Qamar, Raheel and Sarwar, Muhammad T. and Henry, L. Keith and Antonarakis, Stylianos E.. (2020) Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency. Human molecular genetics, 29 (4). pp. 618-623.


Saqib, Muhammad Arif Nadeem and Nikopoulos, Konstantinos and Ullah, Ehsan and Sher Khan, Falak and Iqbal, Jamila and Bibi, Rabia and Jarral, Afeefa and Sajid, Sundus and Nishiguchi, Koji M. and Venturini, Giulia and Ansar, Muhammad and Rivolta, Carlo. (2015) Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophies. Scientific Reports, 5. 09965.

This list was generated on Sat Dec 2 11:01:36 2023 CET.