Associated Papers
Whole Exome Sequencing as a Diagnostic Tool for Unidentified Muscular Dystrophy in a Vietnamese Family.
Nguyen NL et al.
Diagnostics (basel, Switzerland), 2020
32987775 (PubMed )
Supplement: diagnostics-10-00741-s001.zip › diagnostics-900787-supp-xml-2 › Supplementary_Table_S2.xlsx › Sheet1
Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population.
Ren X et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2010
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