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Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3AG mutation that causes exon skipping
Madsen PP,
Kibæk M,
Roca X,
Sachidanandam R,
Krainer AR,
Christensen E,
Steiner RD,
Gibson KM,
Corydon TJ,
Knudsen I,
Wanders RJ,
Ruiter JP,
Gregersen N,
Andresen BS

Human Genetics
  118 (6): 680-690; 2006  
[Abstract]
[DOI] [Full Text] [PDF]


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