DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration
Vig, Anjali ; Poulter, James A ; Ottaviani, Daniele ; Tavares, Erika ; Toropova, Katerina ; Tracewska, Anna Maria ; Mollica, Antonio ; Kang, Jasmine ; Kehelwathugoda, Oshini ; Paton, Tara ; Maynes, Jason T ; Wheway, Gabrielle ; Arno, Gavin ; Khan, Kamron N ; McKibbin, Martin ; Toomes, Carmel ; Ali, Manir ; Di Scipio, Matteo ; Li, Shuning ; Ellingford, Jamie ; Black, Graeme ; Webster, Andrew ; Rydzanicz, Małgorzata ; Stawiński, Piotr ; Płoski, Rafał ; Vincent, Ajoy ; Cheetham, Michael E ; Inglehearn, Chris F ; Roberts, Anthony ; Heon, Elise
Genetics in medicine, 2020-12, Vol.22 (12), p.2041-2051 [Periódico revisado por pares]United States: Elsevier Limited
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