๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Dominant Intermediate Charcot-Marie-Tooth Neuropathy Maps to Chromosome 19p12-p13.2

โœ Scribed by M.L. Kennerson; D. Zhu; R.J.M. Gardner; E. Storey; J. Merory; S.P. Robertson; G.A. Nicholson


Book ID
117853715
Publisher
American Society of Human Genetics
Year
2001
Tongue
English
Weight
913 KB
Volume
69
Category
Article
ISSN
0002-9297

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Charcot-marie-tooth neuropathy related t
โœ Ionasescu, Victor V. ;Trofatter, James ;Haines, Jonathan L. ;Ionasescu, Rebecca ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 439 KB

One family with documented male-to-male transmission of Charcot-Marie-Tooth (CMT) neuropathy was studied clinically and by genetic linkage. Patients had progressive distal weakness and atrophy, areflexia, and distal sensory loss, but early onset (before age 3 years) in all 5 cases, and phrenic nerve

The human VAV proto-oncogene maps to chr
โœ Cecile Martinerie; Linda A. Cannizzaro; Carlo M. Croce; Kay Huebner; Shulamit Ka ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer ๐ŸŒ English โš– 576 KB

A novel human oncogene, designated VAV, has been recently characterized. This oncogene was generated by a rearrangement within the 5' coding sequences of a normal cellular gene, the VAV proto-oncogene. The normal VAV gene is specifically expressed in hematopoietic cells regardless of their different