Tsai Т.Е. et al. 1999


Tsai Т.Е., Jiang Y.H., Bressler J., Armstrong D., and Beaudet A.L., 1999. Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome. Hum. Mol. Genet. 8: 1357-1364.

Смотрите также:

  • Эпигенетика и синдромы Прадера-Уилли (PWS) и Ангелмана (AS)