Menardi C.,1997


Menardi C., Schneider R., Neuschmid-Kaspar F., Klocker H., Hirsch-Kauffmann M., Auer B., Schweiger M. Human APRT deficiency: indication for multiple origins of the most common Caucasian mutation and detection of a novel type of mutation involving intrastrand-templated repair. - Hum.Mut., 1997, v. 10, p. 251-255.

Смотрите также:

  • Табл. APRT m