Progress in the elucidation of the genetic basis for inherited peripheral neuropathies has been remarkable over the last years. In particular, the molecular mechanisms underlying the autosomal dominantly inherited disorders Charcot-Marie-Tooth disease type 1A (CMT 1 A), Charcot-Marie-Tooth disease t
β¦ LIBER β¦
Molecular genetic basis of primary inherited optic neuropathies
β Scribed by Votruba, M
- Book ID
- 110035659
- Publisher
- Nature Publishing Group
- Year
- 2004
- Tongue
- English
- Weight
- 103 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0950-222X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Genetic basis of inherited peripheral ne
β
Ueli Suter; Pragna I. Patel
π
Article
π
1994
π
John Wiley and Sons
π
English
β 772 KB
Pathology and molecular genetics of inhe
β
Christopher J Klein
π
Article
π
2004
π
Elsevier Science
π
English
β 68 KB
Molecular mechanisms of inherited demyel
β
Steven S. Scherer; Lawrence Wrabetz
π
Article
π
2008
π
John Wiley and Sons
π
English
β 360 KB
## Abstract The past 15 years have witnessed the identification of more than 25 genes responsible for inherited neuropathies in humans, many associated with primary alterations of the myelin sheath. A remarkable body of work in patients, as well as animal and cellular models, has defined the clinic
Molecular genetic basis of inherited cat
β
M.Ashwin Reddy; Peter J Francis; Vanita Berry; Shomi S Bhattacharya; Anthony T M
π
Article
π
2004
π
Elsevier Science
π
English
β 446 KB
Genetic Screening for OPA1 and OPA3 Muta
β
Patrick Yu-Wai-Man; Suma P. Shankar; ValΓ©rie Biousse; Neil R. Miller; Lora J.H.
π
Article
π
2011
π
Elsevier Science
π
English
β 401 KB
A review of primary hereditary optic neu
β
M. Votruba; S. Aijaz; A. T. Moore
π
Article
π
2003
π
Springer
π
English
β 188 KB