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Volumn 22, Issue 25, 2013, Pages 5229-5236

Congenital myopathy is caused by mutation of HACD1

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COA DEHYDRATASE 1; 3 HYDROXYACYL COENZYME A DEHYDROGENASE; BETA SARCOGLYCAN; CAVEOLIN 3; COLLAGEN TYPE 4; COLLAGEN TYPE 6; DELTA SARCOGLYCAN; DYSFERLIN; DYSTROPHIN; EMERIN; GAMMA SARCOGLYCAN; LAMININ; MEMBRANE LIPID; MEROSIN; MESSENGER RNA; PERLECAN; SARCOGLYCAN; SPECTRIN; UNCLASSIFIED DRUG; UTROPHIN; VERY LONG CHAIN FATTY ACID;

EID: 84888788970     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt380     Document Type: Article
Times cited : (43)

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