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Elsevier, Genetics in Medicine, 12(22), p. 2041-2051, 2020

DOI: 10.1038/s41436-020-0915-1

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DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration

Journal article published in 2020 by Anjali Vig, James A. Poulter, Daniele Ottaviani, Erika Tavares, Katerina Toropova, Anna Maria Tracewska, Antonio Mollica, Jasmine Kang, Oshini Kehelwathugoda, Tara Paton, Jason T. Maynes, Gabrielle Wheway, Gavin Arno, J. C. Ambrose, P. Arumugam and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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