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Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
1061-4036
595-600
Klein, Christopher J.
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Botuyan, Maria-Victoria
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Wu, Yanhong
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Ward, Christopher J.
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Nicholson, Garth A.
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Hammans, Simon
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Hojo, Kaori
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Yamanishi, Hiromitch
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Karpf, Adam R.
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Wallace, Douglas C.
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Simon, Mariella
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Lander, Cecilie
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Boardman, Lisa A.
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Cunningham, Julie M.
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Smith, Glenn E.
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Litchy, William J.
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Boes, Benjamin
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Atkinson, Elizabeth J.
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Middha, Sumit
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B Dyck, P. James
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Parisi, Joseph E.
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Mer, Georges
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Smith, David I.
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Dyck, Peter J.
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Klein, Christopher J.
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Botuyan, Maria-Victoria
0de6ac2f-6d27-493a-b0b7-2df45367c3c3
Wu, Yanhong
d41d61c3-5b59-474f-9c5b-cd0c27dc2399
Ward, Christopher J.
c52417ba-332a-40dc-8c6a-fe593b26f688
Nicholson, Garth A.
8361a66b-4a9f-46c7-811f-a85c784c6bd6
Hammans, Simon
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Hojo, Kaori
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Yamanishi, Hiromitch
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Karpf, Adam R.
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Wallace, Douglas C.
c24023ec-2f46-463d-9110-85863808b290
Simon, Mariella
b8b186fc-f7ea-4dd0-938c-b5c39be6497c
Lander, Cecilie
8d095eea-e45d-4b05-a5a0-a1cfdacc7949
Boardman, Lisa A.
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Cunningham, Julie M.
6181118b-0b2c-4af9-8d8e-241b76808ca8
Smith, Glenn E.
999e31e2-e5f4-4a23-814e-90e892142fd3
Litchy, William J.
d1cb52cf-a302-4df9-b387-00b1e2c32f53
Boes, Benjamin
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Atkinson, Elizabeth J.
a727fce0-ab34-4e9c-ade1-f7a5c983fa89
Middha, Sumit
69f386d2-73f3-46d7-9eaf-044915ca952a
B Dyck, P. James
ae9d0504-c187-4224-8270-f624f3f3bb6f
Parisi, Joseph E.
b388ceac-0692-4b98-b687-7942f7d42748
Mer, Georges
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Smith, David I.
78443203-9793-4aba-a1f7-022281de9431
Dyck, Peter J.
aa24f29a-eb87-494f-a069-c0f3973d1c35

Klein, Christopher J., Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J., Nicholson, Garth A., Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R., Wallace, Douglas C., Simon, Mariella, Lander, Cecilie, Boardman, Lisa A., Cunningham, Julie M., Smith, Glenn E., Litchy, William J., Boes, Benjamin, Atkinson, Elizabeth J., Middha, Sumit, B Dyck, P. James, Parisi, Joseph E., Mer, Georges, Smith, David I. and Dyck, Peter J. (2011) Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. Nature Genetics, 43 (6), 595-600. (doi:10.1038/ng.830).

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Published date: 1 May 2011
Organisations: Human Development & Health

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Local EPrints ID: 337666
URI: http://eprints.soton.ac.uk/id/eprint/337666
ISSN: 1061-4036
PURE UUID: 374f90b6-e554-40d9-be32-7102c276f2e5

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Date deposited: 01 May 2012 13:53
Last modified: 14 Mar 2024 10:56

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Contributors

Author: Christopher J. Klein
Author: Maria-Victoria Botuyan
Author: Yanhong Wu
Author: Christopher J. Ward
Author: Garth A. Nicholson
Author: Simon Hammans
Author: Kaori Hojo
Author: Hiromitch Yamanishi
Author: Adam R. Karpf
Author: Douglas C. Wallace
Author: Mariella Simon
Author: Cecilie Lander
Author: Lisa A. Boardman
Author: Julie M. Cunningham
Author: Glenn E. Smith
Author: William J. Litchy
Author: Benjamin Boes
Author: Elizabeth J. Atkinson
Author: Sumit Middha
Author: P. James B Dyck
Author: Joseph E. Parisi
Author: Georges Mer
Author: David I. Smith
Author: Peter J. Dyck

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