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Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death.

Document Type

Article

Author

Cao, Siqi; Smith, Laura L.; Padilla-Lopez, Sergio R.; Guida, Brandon S.; Blume, Elizabeth; Shi, Jiahai; Morton, Sarah U.; Brownstein, Catherine A.; Beggs, Alan H.; Kruer, Michael C.; Agrawal, Pankaj B.

Source

Human Molecular Genetics; 9/15/2017, Vol. 26 Issue 18, p3545-3552, 8p

Subject

Language

ISSN

09646906

Online Access

Full Text (Oxford University Press) Full Text (OUP Near Archive) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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