Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease

AJ Churchill, NJ Marchbank, J Craig, J Leek, M Toohey, AJ Markham, D Mackey, C Toomes, CF Inglehearn

Research output: Contribution to journalArticle (Academic Journal)

Translated title of the contributionDeletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease
Original languageEnglish
Pages (from-to)47 - 48
JournalJournal of Medical Genetics
Volume39
Publication statusPublished - 2002

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