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Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.
Am J Hum Genet. 1999 Feb;64(2):479-94. doi: 10.1086/302261.
Am J Hum Genet. 1999.
PMID: 9973285
Free PMC article.
Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood.
Strauss AW, Powell CK, Hale DE, Anderson MM, Ahuja A, Brackett JC, Sims HF.
Strauss AW, et al.
Proc Natl Acad Sci U S A. 1995 Nov 7;92(23):10496-500. doi: 10.1073/pnas.92.23.10496.
Proc Natl Acad Sci U S A. 1995.
PMID: 7479827
Free PMC article.
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