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Diagnosis of autosomal dominant optic atrophy plus syndrome and classic type (OPA1 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 13/12/2016
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Last update: December 2016

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of genes tested (including panels) (1)
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