Novel homozygous OPA3 mutation in an Afghani family with 3-methylglutaconic aciduria type III and optic atrophy

Title
Novel homozygous OPA3 mutation in an Afghani family with 3-methylglutaconic aciduria type III and optic atrophy
Authors
Keywords
-
Journal
OPHTHALMIC GENETICS
Volume 40, Issue 6, Pages 570-573
Publisher
Informa UK Limited
Online
2020-01-13
DOI
10.1080/13816810.2019.1711428

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