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Q32161682-DA4FBF93-CBC2-4187-91A4-7BFD74BBEA74
Q32161682-DA4FBF93-CBC2-4187-91A4-7BFD74BBEA74
BestRank
Statement
http://www.wikidata.org/entity/statement/Q32161682-DA4FBF93-CBC2-4187-91A4-7BFD74BBEA74
Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).
P2860
Q32161682-DA4FBF93-CBC2-4187-91A4-7BFD74BBEA74
BestRank
Statement
http://www.wikidata.org/entity/statement/Q32161682-DA4FBF93-CBC2-4187-91A4-7BFD74BBEA74
rank
NormalRank
type
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Statement
wasDerivedFrom
96899056bb3aab90d8c2a164abc484c70336946d
P2860
Possible X linked congenital mitochondrial cardiomyopathy in three families