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Q42538852-E3E4557F-5902-4965-84AF-7DCDB3E53E48
Q42538852-E3E4557F-5902-4965-84AF-7DCDB3E53E48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-E3E4557F-5902-4965-84AF-7DCDB3E53E48
'Behr syndrome' with OPA1 compound heterozygote mutations.
P2860
Q42538852-E3E4557F-5902-4965-84AF-7DCDB3E53E48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-E3E4557F-5902-4965-84AF-7DCDB3E53E48
rank
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type
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wasDerivedFrom
54d0087ae6b30278899a272aa58f1532fe8cc966
P2860
Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier