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Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients

Prader-Willi (PWS) and Angelman (AS) syndromes are two clinically distinct genetic diseases associated with multiple physical and cognitive abnormalities. The genetic cause of PWS and AS is the alteration in the 15q11.2-q13 chromosomal region; expression of genes in this region is subject to genome...

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Veröffentlicht in:	Вiopolymers and Cell
Datum:	2018
Hauptverfasser:	Chernushyn, S.Yu., Hryshchenko, N.V.
Format:	Artikel
Sprache:	Englisch
Veröffentlicht:	Інститут молекулярної біології і генетики НАН України 2018
Schlagworte:	Biomedicine
Online Zugang:	https://nasplib.isofts.kiev.ua/handle/123456789/154359
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!
Назва журналу:	Digital Library of Periodicals of National Academy of Sciences of Ukraine
Zitieren:	Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients / S.Yu. Chernushyn, N.V. Hryshchenko // Вiopolymers and Cell. — 2018. — Т. 34, № 5. — С. 361-366. — Бібліогр.: 11 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine

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