OALib Journal期刊
ISSN: 2333-9721
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Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice
DOI: 10.1371/journal.pgen.1008130
Alexander E. Katz, Ayse Bilge Ozel, Ben Emery, Biliana Veleva-Rotse, Cheng-mao Lin, Frank W. Rozsa, Graeme C.M. Black, Gregory L. Skuta, Hemant S. Pawar, James Eadie, Jill E. Urquhart, Julia E. Richards, Jun Z. Li, Laryssa A. Huryn, Laurel Wiinikka-Buesser, Lev Prasov, Louise C. Pyle, Michael Boehnke, Michelle L. Brinkmeier, Mohammad I. Othman, Robert A. Sisk, Robert B. Hufnagel, Sally A. Camper, Sarah J. Garnai, Sarah Sheskey, Sayoko E. Moroi, Scot A. Sullivan, Steven M. Archer, The Genomic Ascertainment Cohort, Tomas S. Aleman
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