Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: A genotype-phenotype correlation [1]

A. A. Yamak; F. Bitar; P. Karam; G. Nemer

doi:10.1111/j.1399-0004.2007.00814.x

Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: A genotype-phenotype correlation [1]

A. A. Yamak, F. Bitar, P. Karam, G. Nemer^*

^*Corresponding author for this work

American University of Beirut

Research output: Contribution to journal › Letter › peer-review

24 Citations (Scopus)

Original language	English
Pages (from-to)	59-62
Number of pages	4
Journal	Clinical Genetics
Volume	72
Issue number	1
DOIs	https://doi.org/10.1111/j.1399-0004.2007.00814.x
Publication status	Published - Jul 2007
Externally published	Yes

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title = "Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: A genotype-phenotype correlation [1]",

author = "Yamak, {A. A.} and F. Bitar and P. Karam and G. Nemer",

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AU - Nemer, G.

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JO - Clinical Genetics

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Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: A genotype-phenotype correlation [1]

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