Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes.

Autor: Heimdörfer, David1 (AUTHOR) david.heimdoerfer@i-med.ac.at, Vorleuter, Alexander1 (AUTHOR), Eschlböck, Alexander2 (AUTHOR), Spathopoulou, Angeliki2 (AUTHOR), Suarez-Cubero, Marta2 (AUTHOR), Farhan, Hesso3 (AUTHOR), Reiterer, Veronika3 (AUTHOR), Spanjaard, Melanie4 (AUTHOR), Schaaf, Christian P.4 (AUTHOR), Huber, Lukas A.5 (AUTHOR), Kremser, Leopold6 (AUTHOR), Sarg, Bettina6 (AUTHOR), Edenhofer, Frank2 (AUTHOR), Geley, Stephan3 (AUTHOR), de Araujo, Mariana E.G.5 (AUTHOR), Huettenhofer, Alexander1 (AUTHOR) alexander.huettenhofer@i-med.ac.at
Zdroj: American Journal of Human Genetics. Jul2024, Vol. 111 Issue 7, p1383-1404. 22p.
Databáze: Academic Search Ultimate