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Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype–phenotype correlation
Author(s) -
Yamak AA,
Bitar F,
Karam P,
Nemer G
Publication year - 2007
Publication title -
clinical genetics
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2007.00814.x
Subject(s) - medicine , pediatrics , emergency department , family medicine , psychiatry