Genes to predict VO(2max) trainability: a systematic review

por Williams, Camilla J., Williams, Mark G., Eynon, Nir, Ashton, Kevin J., Little, Jonathan P., Wisloff, Ulrik, Coombes, Jeff S.
Publicado 2017

Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations

por Bossuyt, Stijn N V, Punt, A Mattijs, de Graaf, Ilona J, van den Burg, Janny, Williams, Mark G, Heussler, Helen, Elgersma, Ype, Distel, Ben
Publicado 2021