𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease)

✍ Scribed by P. Scheltens; R. P. M. Bruyn; G. J. Hazenberg

Book ID
114783318
Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
465 KB
Volume
82
Category
Article
ISSN
0001-6314

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Extensive genetic heterogeneity in the “
Extensive genetic heterogeneity in the “pure” form of autosomal dominant familial spastic paraplegia (Strümpell's disease)
✍ Hisashi Kobayashi; Carlos A. Garcia; Puei-Nam Tay; Eric P. Hoffman 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 312 KB 👁 2 views

Three dominantly inherited "pure" form of familial spastic paraplegia (FSP) genes have been genetically mapped to regions of chromosomes, yet no specific genes or mutations have been identified (FSPI ; chromosome 14q, FSP2; chromosome 2p and FSP3; chromosome 15q). We studied a "pure" form of autosom

Genetic anticipation in a large family w
Genetic anticipation in a large family with pure autosomal dominant hereditary spastic paraplegia
✍ Thurmon, T.F.; He, Ching; Haskell, Carroll; Thorpe, Patricia; Thurmon, S.G.; Ros 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 26 KB 👁 2 views

We have reinvestigated a large kindred identified over 25 years ago segregating for a form of pure autosomal dominant hereditary spastic paraplegia (HSP). We have examined additional relatives in order to refine the clinical and genetic characteristics of this disorder, and performed an analysis to