Comment on

• Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.

  Hiltunen T, Kiuru S, Hongell V, Heliö T, Palo J, Peltonen L. Hiltunen T, et al. Am J Hum Genet. 1991 Sep;49(3):522-8. Am J Hum Genet. 1991. PMID: 1652889 Free PMC article.
• APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.

  Schellenberg GD, Anderson L, O'dahl S, Wisjman EM, Sadovnick AD, Ball MJ, Larson EB, Kukull WA, Martin GM, Roses AD, et al. Schellenberg GD, et al. Am J Hum Genet. 1991 Sep;49(3):511-7. Am J Hum Genet. 1991. PMID: 1679288 Free PMC article.
• DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type).

  Bakker E, van Broeckhoven C, Haan J, Voorhoeve E, van Hul W, Levy E, Lieberburg I, Carman MD, van Ommen GJ, Frangione B, et al. Bakker E, et al. Am J Hum Genet. 1991 Sep;49(3):518-21. Am J Hum Genet. 1991. PMID: 1679289 Free PMC article.