Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene.

M Muglia, A Toscano, A L Gabriele, A Magariello, A Patitucci, F L Conforti, R Mazzei, C Rodolico, A Gambardella, A Quattrone

Journal: Human mutation 2000;15(3):299

PMID: 10679959

Abstract

Address: Institute of Experimental Medicine and Biotechnology, National Research Council, Piano Lago di Mangone, Cosenza. [email protected]

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MeSH Terms: Amino Acid Substitution, Arginine, Charcot-Marie-Tooth Disease, Glutamine, Humans, Male, Middle Aged, Molecular Sequence Data, Myelin P0 Protein, Polymerase Chain Reaction, Polymorphism, Genetic, Polymorphism, Single-Stranded Conformational