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Q49119860-044353D6-E0C8-41BD-88ED-0B477B870A2C
Q49119860-044353D6-E0C8-41BD-88ED-0B477B870A2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49119860-044353D6-E0C8-41BD-88ED-0B477B870A2C
Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature child.
P2860
Q49119860-044353D6-E0C8-41BD-88ED-0B477B870A2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49119860-044353D6-E0C8-41BD-88ED-0B477B870A2C
rank
NormalRank
type
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Statement
wasDerivedFrom
a159f72089e8f82d9b1836ea420060044fb824b0
P2860
Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy