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OPTIC ATROPHY 6 (disorder)

Known as: OPA6, OPTIC ATROPHY 6, Optic atrophy, congenital or early infantile, autosomal recessive 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal recessive inheritanceColor Blindness, Red-GreenOPA6 gene

Broader (1)

Optic Atrophies, Hereditary

Papers overview

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2012
2012
TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy
Purpose Nonsyndromic autosomal recessive optic atrophy (arOA) is extremely rare and its existence was disputed until a locus… 
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