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Q42538852-7D6A395B-D5CC-40CD-AFDE-CBDD05716CF7
Q42538852-7D6A395B-D5CC-40CD-AFDE-CBDD05716CF7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-7D6A395B-D5CC-40CD-AFDE-CBDD05716CF7
'Behr syndrome' with OPA1 compound heterozygote mutations.
P2860
Q42538852-7D6A395B-D5CC-40CD-AFDE-CBDD05716CF7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-7D6A395B-D5CC-40CD-AFDE-CBDD05716CF7
rank
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type
BestRank
Statement
wasDerivedFrom
54d0087ae6b30278899a272aa58f1532fe8cc966
P2860
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes