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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Advances in Oncolytic Viral Therapy in Melanoma: A Comprehensive Review by Ayushi Garg, Rohit Rao, Felicia Tejawinata, Gazi Amena Noor Shamita, McKay S. Herpel, Akihiro Yoshida, Gordon Goolamier, Jessica Sidiropoulos, Iris Y. Sheng, Salim-Tamuz Abboud, Luke D. Rothermel, Nami Azar, Ankit Mangla

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Evolution of vitelliform maculopathy in a pediatric patient with a homozygous RP1L1 variant by Alessia Amato, Paul Yang

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