A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy

David B. Parkinson; Peter Arthur-Farraj; Kristjan R. Jessen; Rhona Mirsky

doi:10.1016/j.nbd.2006.06.006

A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy

David B. Parkinson, Peter Arthur-Farraj, Kristjan R. Jessen^*, Rhona Mirsky

^*Corresponding author for this work

Peninsula Medical School

University College London

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

Original language	English
Pages (from-to)	159-169
Number of pages	0
Journal	Neurobiology of Disease
Volume	24
Issue number	1
DOIs	https://doi.org/10.1016/j.nbd.2006.06.006
Publication status	Published - Mar 2006

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10.1016/j.nbd.2006.06.006

Cite this

@article{9bb62533d3cf45ad9d35b4fc3b794811,

title = "A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy",

author = "Parkinson, {David B.} and Peter Arthur-Farraj and Jessen, {Kristjan R.} and Rhona Mirsky",

year = "2006",

month = mar,

doi = "10.1016/j.nbd.2006.06.006",

language = "English",

volume = "24",

pages = "159--169",

journal = "Neurobiology of Disease",

issn = "0969-9961",

publisher = "Academic Press Inc.",

number = "1",

}

Parkinson, DB, Arthur-Farraj, P, Jessen, KR & Mirsky, R 2006, 'A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy', Neurobiology of Disease, vol. 24, no. 1, pp. 159-169. https://doi.org/10.1016/j.nbd.2006.06.006

A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy. / Parkinson, David B.; Arthur-Farraj, Peter; Jessen, Kristjan R. et al.
In: Neurobiology of Disease, Vol. 24, No. 1, 03.2006, p. 159-169.

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

TY - JOUR

T1 - A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy

AU - Parkinson, David B.

AU - Arthur-Farraj, Peter

AU - Jessen, Kristjan R.

AU - Mirsky, Rhona

PY - 2006/3

Y1 - 2006/3

U2 - 10.1016/j.nbd.2006.06.006

DO - 10.1016/j.nbd.2006.06.006

M3 - Article

SN - 0969-9961

VL - 24

SP - 159

EP - 169

JO - Neurobiology of Disease

JF - Neurobiology of Disease

IS - 1

ER -