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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10.1111/j.1399-0004.2007.00814.x

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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",

year = "2007",

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language = "English",

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T1 - Exclusive cardiac dysfunction in familial primary carnitine deficiency cases

T2 - A genotype-phenotype correlation [1]

AU - Yamak, A. A.

AU - Bitar, F.

AU - Karam, P.

AU - Nemer, G.

PY - 2007/7

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UR - https://www.scopus.com/pages/publications/34347343996

U2 - 10.1111/j.1399-0004.2007.00814.x

DO - 10.1111/j.1399-0004.2007.00814.x

M3 - Letter

C2 - 17594400

AN - SCOPUS:34347343996

SN - 0009-9163

VL - 72

SP - 59

EP - 62

JO - Clinical Genetics

JF - Clinical Genetics

IS - 1

ER -

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

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