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

Tohru Ikegami; Garth Nicholson; Hiroyuki Ikeda; Akihiro Ishida; Heather Johnston; Grahame Wise; Robert Ouvrier; Kiyoshi Hayasaka

doi:10.1002/humu.1380110134

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

Tohru Ikegami, Garth Nicholson, Hiroyuki Ikeda, Akihiro Ishida, Heather Johnston, Grahame Wise, Robert Ouvrier, Kiyoshi Hayasaka^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

9 Citations (Scopus)

Original language	English
Pages (from-to)	S103-S105
Number of pages	3
Journal	Human Mutation
Volume	11
Issue number	SUPPL 1
DOIs	https://doi.org/10.1002/humu.1380110134
Publication status	Published - 1998
Externally published	Yes

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title = "De novo mutation of the myelin po gene in d{\'e}j{\'e}rine-sottas disease (hereditary motor and sensory neuropathy type III): Two amino acid insertion after Asp 118",

author = "Tohru Ikegami and Garth Nicholson and Hiroyuki Ikeda and Akihiro Ishida and Heather Johnston and Grahame Wise and Robert Ouvrier and Kiyoshi Hayasaka",

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AU - Ikegami, Tohru

AU - Nicholson, Garth

AU - Ikeda, Hiroyuki

AU - Ishida, Akihiro

AU - Johnston, Heather

AU - Wise, Grahame

AU - Ouvrier, Robert

AU - Hayasaka, Kiyoshi

PY - 1998

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DO - 10.1002/humu.1380110134

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AN - SCOPUS:0031984943

SN - 1059-7794

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SP - S103-S105

JO - Human Mutation

JF - Human Mutation

IS - SUPPL 1

ER -

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

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