PEX6 Mutations in Peroxisomal Biogenesis Disorders

PEX6 Mutations in Peroxisomal Biogenesis Disorders

Purpose: Peroxisomal biogenesis disorders (PBDs) represent a spectrum of conditions that result in vision loss, sensorineural hearing loss, neurologic dysfunction, and other abnormalities resulting from aberrant peroxisomal function caused by mutations in PEX genes. With no treatments currently avai...

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Bibliographic Details
Main Authors:	Matthew D. Benson, MD, Kimberly M. Papp, BSc, Geoffrey A. Casey, BSc(EE), BSc(MolBiol), Alina Radziwon, BSc, Chris D. St Laurent, BSc, Lance P. Doucette, PhD, Ian M. MacDonald, MD, CM
Format:	Article
Language:	English
Published:	Elsevier 2021-06-01
Series:	Ophthalmology Science
Subjects:	Hearing loss Peroxisomal biogenesis disorders Peroxisome PEX6 Retinal degeneration Usher syndrome
Online Access:	http://www.sciencedirect.com/science/article/pii/S2666914521000269

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