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Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing https://t.co/IgryPEuwMR https://t.co/dFq1gojH2s
Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing https://t.co/IgryPEuwMR https://t.co/dFq1gojH2s
Novel rare skin mutation gene identified by whole exome sequencing https://t.co/gswvwWstLs https://t.co/5VAXrmmchC