Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease - PubMed (original) (raw)
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease
N J Marchbank et al. J Med Genet. 2002 Aug.
No abstract available
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