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.
| Autor: | Shah, Jhanvi1 (AUTHOR), Patel, Harsh2 (AUTHOR), Jain, Deepika3 (AUTHOR), Sheth, Frenny1 (AUTHOR) frenny.sheth@frige.co.in, Sheth, Harsh1 (AUTHOR) harsh.sheth@frige.co.in |
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| Zdroj: | BMC Neurology. 12/2/2021, Vol. 21 Issue 1, p1-8. 8p. |
| Databáze: | Academic Search Ultimate |
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