๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Charcot-Marie-Tooth disease type 1 and 2: analysis of sensory dysfunction with quantitative determination of somatosensory thresholds

โœ Scribed by U.B. Ericson; K. Borg


Book ID
117670825
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
133 KB
Volume
7
Category
Article
ISSN
0960-8966

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Duplication of part of chromosome 17 is
โœ P. J. Hallam; A. E. Harding; J. Berciano; D. F. Barker; Dr S. Malcolm ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 477 KB ๐Ÿ‘ 3 views

Hereditary motor and sensory neuropathy type I (HMSNI), also known as Charcot-Marie-Tooth disease type 1 (CMTl), has been shown to be genetically heterogeneous. A major gene maps to chromosome 17 (CMTlA). A set of loci, D17S122, D17S125, and D17S124, show tight linkage to the C M T l A locus, and a