Dumanchin C.,1998


Dumanchin C., Brice A., Campion D., Hannequin D., Martin C., Moreau V., Agid Y., Martinez M., Clerget-Darpoux F., Frebourg T. De novo presenilin 1 mutation are rare in clinically sporadic early-onset Alzheimer's disease cases. - J.Med.Genet., 1998, v. 35, p. 672-673.

Смотрите также:

  • Табл. PSEN1m