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De novo mutation of the myelin Po gene in Déjérine‐Sottas disease (hereditary motor and sensory neuropathy type III): Two amino acid insertion after Asp 118
Author(s) -
Ikegami Tohru,
Nicholson Garth,
Ikeda Hiroyuki,
Ishida Akihiro,
Johnston Heather,
Wise Grahame,
Ouvrier Robert,
Hayasaka Kiyoshi
Publication year - 1998
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.1380110134
Subject(s) - general hospital , medicine , pediatrics