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Authors
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
Ambrose, J.C.
Arumugam, P.
Baple, E.L.
Bleda, M.
Boardman-Pretty, F.
Boissiere, J.M.
Boustred, C.R.
Brittain, H.
Caulfield, M.J.
Chan, G.C.
Craig, C.E.H.
Daugherty, L.C.
de Burca, A.
Devereau, A.
Elgar, G.
Foulger, R.E.
Fowler, T.
Furió-Tarí, P.
Hackett, J.M.
Halai, D.
Hamblin, A.
Henderson, S.
Holman, J.E.
Hubbard, T.J.P.
Ibáñez, K.
Jackson, R.
Jones, L.J.
Kasperaviciute, D.
Kayikci, M.
Lahnstein, L.
Lawson, K.
Leigh, S.E.A.
Leong, I.U.S.
Lopez, F.J.
Maleady-Crowe, F.
Mason, J.
McDonagh, E.M.
Moutsianas, L.
Mueller, M.
Murugaesu, N.
Need, A.C.
Odhams, C.A.
Patch, C.
Perez-Gil, D.
Polychronopoulos, D.
Pullinger, J.
Rahim, T.
Rendon, A.
Riesgo-Ferreiro, P.
Rogers, T.
Ryten, M.
Savage, K.
Sawant, K.
Scott, R.H.
Siddiq, A.
Sieghart, A.
Smedley, D.
Smith, K.R.
Sosinsky, A.
Spooner, W.
Stevens, H.E.
Stuckey, A.
Sultana, R.
Thomas, E.R.A.
Thompson, S.R.
Tregidgo, C.
Tucci, A.
Walsh, E.
Watters, S.A.
Welland, M.J.
Williams, E.
Witkowska, K.
Wood, S.M.
Zarowiecki, M.
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 https://orcid.org/0000-0003-4143-9311
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Funding
Funding for this research was provided by:
Wellcome Trust (104196/Z/14/Z)
Biotechnology and Biological Sciences Research Council (BB/P008348/1)
Wellcome Trust (204378/Z/16/)
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More Information
This article is maintained by: Elsevier
Article Title: DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-0915-1
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
