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

10 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",

year = "1998",

doi = "10.1002/humu.1380110134",

language = "English",

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T1 - De novo mutation of the myelin po gene in déjérine-sottas disease (hereditary motor and sensory neuropathy type III)

T2 - Two amino acid insertion after Asp 118

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

Y1 - 1998

UR - https://www.scopus.com/pages/publications/0031984943

U2 - 10.1002/humu.1380110134

DO - 10.1002/humu.1380110134

M3 - Article

C2 - 9452055

AN - SCOPUS:0031984943

SN - 1059-7794

VL - 11

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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