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A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome | BMC Neurology https://t.co/lw0nzNDM7A
A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome | BMC Neurology https://t.co/lw0nzNDM7A