𝔖 Bobbio Scriptorium
✦   LIBER   ✦

LDL RECEPTOR MUTATION IN A DRUZE KINDRED- CLINICAL, BIOCHEMICAL AND GENETIC CHARACTERISTICS

✍ Scribed by Pinhas-Hamiel, O.; Wael, N.; Anikster, Y.; Mazor-Aronovitch, K.; Harats, D.; Cohen, H.


Book ID
121903579
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
70 KB
Volume
9
Category
Article
ISSN
1567-5688

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A clinical, genetic, and biochemical cha
✍ Alessia Arnoldi; Alessandra Tonelli; Francesca Crippa; Gaetano Villani; Consigli πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 471 KB πŸ‘ 1 views

Mutations in the SPG7 gene encoding a mitochondrial protein termed paraplegin, are responsible for a recessive form of hereditary spastic paraparesis. Only few studies have so far been performed in large groups of hereditary spastic paraplegia (HSP) patients to determine the frequency of SPG7 mutati