Whole‐exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death

Publisher: John Wiley & Sons Inc

E-ISSN: 1582-4934|22|2|1350-1354

ISSN: 1582-1838

Source: Journal of Cellular and Molecular Medicine, Vol.22, Iss.2, 2018-02, pp. : 1350-1354

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