SCN10A variants associated with congenital Harlequin Syndrome. Halle A, De Becdelievre A, Funalot B, Labreze C, et al. Br J Dermatol 2022 Jan 10. doi: 10.1111/bjd.21011.

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Amedeo Smart

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Halle A, De Becdelievre A, Funalot B, Labreze C, et al. SCN10A variants associated with congenital Harlequin Syndrome. Br J Dermatol 2022 Jan 10. doi: 10.1111/bjd.21011.
PMID: 35007332