Arif O Khan (A O Khan)

Years Active: 2017-2023
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Thales Antonio Cabral de Guimaraes, Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, Ajoy Vincent, Fadi Nasser, Samer Khateb, Omar A Mahroo, Nikolas Pontikos, Maurício E Vargas, Alberta A H J Thiadens, Emanuel R de Carvalho, Xuan-Than-An Nguyen, Gavin Arno, Yu Fujinami-Yokokawa, Xiao Liu, Kazushige Tsunoda, Takaaki Hayashi, Belén Jiménez-Rolando, Maria Inmaculada Martin-Merida, Almudena Avila-Fernandez, Ester Carreño Salas, Blanca Garcia-Sandoval, Carmen Ayuso, Dror Sharon, Susanne Kohl, Rachel M Huckfeldt, Eyal Banin, Mark E Pennesi, Arif O Khan, Bernd Wissinger, Andrew R Webster, Elise Heon, Camiel J F Boon, Eberhard Zrenner, Michel Michaelides
KCNV2 -associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3. The British journal of ophthalmology (2023)
Arif O Khan, B S Budde, P Nürnberg, A Kawalia, S Lenzner, H J Bolz
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotype. Clinical genetics 93 (1) (2017)

Arif O Khan.css-eqlu8i{font-size:small;padding-left:4px;} (A O Khan)