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Kleefstra syndrome and sleep disorders: An Italian case report

<p>Kleefstra Syndrome (KS)is a rare genetic syndrome affecting approximately 1 in 200,000 individuals and is caused by either a deletion of the subtelomeric region of chromosome 9q (50%) or by a loss of function mutation in the Euchromatin Histone Methyl Transferase 1 (EHMT1) gene (50%). In th...

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Bibliografski detalji
Glavni autor:	Ettore Caterino (Autor)
Format:	Knjiga
Izdano:	Journal of Neurology, Neurological Science and Disorders - Peertechz Publications, 2023-06-28.
Teme:	Case Report
Online pristup:	Connect to this object online.
Oznake:	Dodaj oznaku Bez oznaka, Budi prvi tko označuje ovaj zapis!

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