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ARVO Annual Meeting Abstract July 2019

Identification of novel mutations in PITX2 gene in Pakistani and Mexican Families with Axenfeld-Rieger Syndrome

Valeria Lo Faro; Shazia Micheal; Sorath Noorani Siddiqu; Muhammad Imran Khan; Philip Wagstaff; Cristina Villanueva Mendoza; Nomdo M Jansonius; Arthur A Bergen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5428. doi:

ARVO Annual Meeting Abstract July 2019

Towards comprehensive identification and functional characterization of deep-intronic ABCA4 variants in 1000 Stargardt disease cases

Mubeen Khan; Stephanie Cornelis; Marta del Pozo Valero; Muhammad Imran Khan; Heidi Stohr; Felix Grassmann; Marloes Steehouwer; Alexander Hoischen; Carmen Ayuso; Raj Ramesar; Isabelle Anne Meunier; Sabine defoort; Bernhard HF Weber; Claire-Marie Dhaenens; Frans P Cremers

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2813. doi:

ARVO Annual Meeting Abstract July 2019

Next generation sequencing using molecular inversion probes in hereditary retinal disorders genes in Polish patients: an update

Anna M. Tracewska-Siemiatkowska; Joanna Murawska; Beata Kocyla-Karczmarewicz; Marek Szalinski; Agnieszka Rafalska; Malgorzata Rydzanicz; Piotr Stawinski; Elzbieta Ciara; Muhammad Imran Khan; Arjen Henkes; Alexander Hoischen; Christian Gilisen; Maartje van der Vorst; Frans P Cremers; Rafal Ploski; Krystyna Chrzanowska

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2941. doi:

ARVO Annual Meeting Abstract July 2018

A frameshift mutation in RDH12 causes autosomal dominant retinitis pigmentosa in families of Tunisian Jewish origin

Boris Rosin; Prasanthi Namburi; Muhammad Imran Khan; Frans P Cremers; Eyal Banin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1004. doi:

ARVO Annual Meeting Abstract July 2018

Novel mutations in Polish patients with hereditary retinal disorders

Anna Maria Tracewska-Siemiatkowska; Joanna Murawska; Beata Kocyla-Karczmarewicz; Marek Szalinski; Malgorzata Rydzanicz; Piotr Stawinski; Muhammad Imran Khan; Alexander Hoischen; Christian Gilissen; Maartje van de Vorst; Frans P Cremers; Rafal Ploski; Krystyna Chrzanowska

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2324. doi:

ARVO Annual Meeting Abstract June 2015

Identification of the causal variants for different inherited retinal phenotypes in a complex consanguineous family from Pakistan

Maleeha Maria; Maleeha Azam; Syeda Hafiza Benish Ali; Frans Cremers; Raheel Qamar; Muhammad Imran Khan; Lonneke Haer-Wigman

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2859. doi:

ARVO Annual Meeting Abstract March 2012

CYP1B1 Mutations Cause Glaucoma in Pakistani and Saudi Arabian Patients

Shazia Micheal; Humaira Ayub; Muhammad Imran Khan; Farah Akhtar; Mahmood Ali; Robert K Koenekoop; Manal Hedrawi; Osama M Badeeb; Raheel Qamar; Anneke I den Hollander

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4499. doi:

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