A novel mutation ofpresenilin 1in familial Alzheimer’s disease in Israel detected by denaturing gradient gel electrophoresis
✍ Scribed by Haike Reznik-Wolf; Therese A. Treves; Michael Davidson; Judith Aharon-Peretz; Peter H. St. George Hyslop; Joab Chapman; Amos D. Korczyn; Boleslaw Goldman; E. Friedman
- Publisher
- Springer
- Year
- 1996
- Tongue
- English
- Weight
- 47 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
30 cycles, denaturation 94 (1 min) annezling 58 (1 Min.) extension 72 (1 min.), magnesium concentration 1.5mM, electrophoresis: 58 degrees celsius, 16 hours, 80 volts,
Communicated by Kenneth K. Kidd Gennline missense mutations within the coding region of the RET proto-oncogene have recently been described in patients with the dominantly inherited cancer syndromes, multiple endocrine neoplasia type 2a (MEN 2a) and familial medullary thyroid carcinoma (FMTC). To da
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder with an incidence of between 1: 3000 and 1: 4000. Common clinical signs include more than six café-au-lait spots, multiple cutaneous neurofibromas and iris Lisch nodules. Rarer are skeletal anomalies, learning disabilities and an incre