✦ LIBER ✦

Unusual Charcot–Marie–Tooth phenotype due to a mutation within the intracellular domain of myelin protein zero

✍ Scribed by Christiane Schneider-Gold; Judith Kötting; Jörg T. Epplen; Ralf Gold; Wanda M. Gerding

Book ID: 102953309
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 933 KB
Volume: 41
Category: Article
ISSN: 0148-639X
DOI: 10.1002/mus.21523

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Charcot-Marie-Tooth disease due to the T

Charcot-Marie-Tooth disease due to the Thr124Met mutation in the myelin protein zero gene associated with multiple sclerosis

✍ Yusuf A. Rajabally; Richard J. Abbott 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 35 KB

Intermediate Charcot-Marie-Tooth disease

Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic pain

✍ Juan D. Ramirez; Phillip R.J. Barnes; Kerry R. Mills; David L.H. Bennett 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 518 KB

Autonomic and respiratory dysfunction in

Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene

✍ T Stojkovic; J de Seze; O Dubourg; M.C Arne-Bes; S Tardieu; J.C Hache; P Vermers 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 138 KB

Charcot-Marie-Tooth disease type 2 assoc

Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene

✍ Marrosu, M. G.; Vaccargiu, S.; Marrosu, G.; Vannelli, A.; Cianchetti, C.; Munton 📂 Article 📅 1998 🏛 Lippincott Williams and Wilkins 🌐 English ⚖ 634 KB

An axonal form of Charcot-Marie-Tooth di

An axonal form of Charcot-Marie-Tooth disease with a novel missense mutation in the myelin protein zero gene

✍ Andrzej Kochanski; Dagmara Kabzinska; Adam Nowakowski; Hanna Drac; Irena Hausman 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 27 KB

Charcot-Marie-Tooth disease: a novel Tyr

Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ,P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family

✍ Alejandro Leal; Corinna Berghoff; Martin Berghoff; Gerardo Del Valle; Carlos Con 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 359 KB