Heckmann J.,2002


Heckmann J., de Viliers C., Rutherfoord S., Ramesar R., Morris C., Low R., Kalaria R. Novel presenilin 1 mutation with profound nerofibrillary pathology in an indigenous South African family with early-onset Alzheimer's disease. - Neurobiology of Aging, 2002, v. 23 (1S), p. S321.

Смотрите также:

  • Табл. PSEN1m