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Wild, Robert
Ullah, Raja
A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome.
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A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome.
A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome. J Neurol. 2008 Sep; 255(9):1417-8.
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PubMed
subject areas
Charcot-Marie-Tooth Disease
Child, Preschool
Family Health
Female
Humans
Male
Middle Aged
Myelin Proteins
Pedigree
Point Mutation
Young Adult
authors with profiles
Calin Ioan Prodan