High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patients

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Bibliographic Details
Published in:American journal of human genetics 1996-03, Vol.58 (3), p.638-641
Main Authors: Rouger, H, LeGuern, E, Gouider, R, Tardieu, S, Birouk, N, Gugenheim, M, Bouche, P, Agid, Y, Brice, A
Format: Article
Language:English
Subjects:
Base Sequence
Charcot-Marie-Tooth Disease - genetics
Charcot-Marie-Tooth Disease - physiopathology
Codon - genetics
DNA Mutational Analysis
Female
Humans
Letter
Male
Molecular Sequence Data
Myelin P0 Protein - genetics
Pedigree
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ISSN:0002-9297
1537-6605