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October 14, 2004American Journal of Medical Genetics Part AOpen Access

Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine‐responsive cardiomyopathy in Roma families

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Authors

BMBéla MeleghJBJudit BeneGMGábor Mogyorósy

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Melegh et al. (2004) studied this question.

synapsesocial.com/papers/6a9fc00ffeb70227d67c64c3https://doi.org/10.1002/ajmg.a.30207
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