Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype–phenotype correlation
- 26 June 2007
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 72 (1), 59-62
- https://doi.org/10.1111/j.1399-0004.2007.00814.x
Abstract
No abstract availableKeywords
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