Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sandra Simokovic"'
Autor:
H Backhovens, Eva Nelis, Sandra Simokovic, Ann Löfgren, Vincent Timmerman, Christine Van Broeckhoven, Jean-Jacques Martin, Peter De Jonghe
Publikováno v:
Human mutation
Autor:
Eva Nelis, Sandra Simokovic, Vincent Timmerman, Ann Löfgren, Hubert Backhovens, Peter De Jonghe, Jean‐Jacques Martin, Christine Van Broeckhoven
Publikováno v:
Human Mutation. 9:47-52
Autor:
Sandra Simokovic, Peter De Jonghe, Eva Nelis, Jean-Jacques Martin, Christine Van Broeckhoven, Chantal Ceuterick, Vincent Timmerman, Ann Löfgren, Joke Beuten
Publikováno v:
Human molecular genetics
The distal hereditary motor neuropathy (distal HMN) or the spinal form of Charcot-Marie-Tooth (CMT) disease is an exclusively motor disorder of the peripheral nervous system. The disorder clinically resembles the hereditary motor and sensory neuropat
Autor:
J. J. Martin, C. Van Broeckhoven, Vincent Timmerman, Sandra Simokovic, P. De Jonghe, Jeffery M. Vance, P. Spoelders, Eva Nelis, Ann Löfgren
Publikováno v:
Neurology
Scopus-Elsevier
Scopus-Elsevier
A locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2A) was assigned by linkage analysis to chromosome 1p35-p36. We examined 11 unrelated CMT2 families for linkage to CMT2A using short tandem repeat (STR) polymorphisms. Only one fam