Exome sequencing identifies a homozygous splice site variant in RP1 as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani family by Abdur Rashid, Asad Munir, Muhammad Zahid, Mukhtar Ullah, Atta Ur Rehman

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Identification of new families and variants in autosomal dominant macular dystrophy associated with THRB by Lidia Fernández-Caballero, Fiona Blanco-Kelly, Saoud Tahsin Swafiri, María Inmaculada Martín-Mérida, Mathieu Quinodoz, Mukhtar Ullah, Ester Carreño, María Pilar Martin-Gutierrez, Blanca García-Sandoval, Pablo Minguez, Carlo Rivolta, Marta Corton, Carmen Ayuso

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A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort by Mukhtar Ullah, Atta Ur Rehman, Mathieu Quinodoz, Abdur Rashid, Francesca Cancellieri, Asad Munir, Karolina Kaminska, Afia Iqbal, Samra Javed, Muhammad Dawood, Hafiz Muhammad Azhar Baig, Shamim Saleha, Shagufta Naz, Humera Kausar, Ali Muhammad Waryah, Andrea Superti-Furga, Muhammad Ansar, Carlo Rivolta

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