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Q40719070-53F9144C-EE64-452E-9167-01AB1DD403C3
Q40719070-53F9144C-EE64-452E-9167-01AB1DD403C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40719070-53F9144C-EE64-452E-9167-01AB1DD403C3
Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome.
P2860
Q40719070-53F9144C-EE64-452E-9167-01AB1DD403C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40719070-53F9144C-EE64-452E-9167-01AB1DD403C3
rank
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Statement
wasDerivedFrom
f01ee8d5c361afd0e9eac40fb08f1b8555e6a18c
P2860
Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).