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Q28586216-316141A6-5BAD-45D5-9635-3C079F70D62F
Q28586216-316141A6-5BAD-45D5-9635-3C079F70D62F
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http://www.wikidata.org/entity/statement/Q28586216-316141A6-5BAD-45D5-9635-3C079F70D62F
The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy
P2860
Q28586216-316141A6-5BAD-45D5-9635-3C079F70D62F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28586216-316141A6-5BAD-45D5-9635-3C079F70D62F
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wasDerivedFrom
17ef35304c6670d69ce48488a931655592cc36c0
P2860
Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency.