Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature

Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):594-603.DOI:10.1167/iovs.16-21026

Taylor RL, Handley MT, Waller S, Campbell C, Urquhart J, Meynert AM, Ellingford JM, Donnelly D, Wilcox G, Lloyd IC, Mundy H, FitzPatrick DR,Deshpande C, Clayton-Smith J Black GC

https://www.ncbi.nlm.nih.gov/pubmed?term=%22Investigative+ophthalmology+%26+visual+science%22%5BJour%5D+AND+58%5Bvolume%5D+AND+1%5Bissue%5D+AND+594%5Bpage%5D+AND+2017%5Bpdat%5D&cmd=detailssearch

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