Language
English
German
^M
Dutch
Spanish
Title:
Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance
Source:
Human Molecular Genetics [0964-6906] Humble, M M yr:2013
Basic
Sorry, no full text available...
Please use the document delivery service (see below)
Holding information
Holdings in library search engine
ALBERT
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Saneto, Russell P.
"Alpers-huttenlocher syndrome."
Pediatric neurology
48.3 (2013): 167-178.
description
2.
Ferri, L.
"New clinical and molecular insights on Barth syndrome."
Orphanet journal of rare diseases
8.1 (2013): 27-27.
description
3.
Woodbridge, P.
"POLG mutations in Australian patients with mitochondrial disease."
Internal medicine journal
43.2 (2012): 150-156.
description
4.
Mayr, Johannes A.
"Lack of the mitochondrial protein acylgylcerol kinase causes sengers syndrome.(Report)."
American journal of human genetics
90.2 (2012): 314-.
description
5.
Pronicka, E.
"Drug-resistant epilepsia and fulminant valproate liver toxicity. Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p.W748S mutation in POLG gene."
Medical Science Monitor
17.4 (2011): 203-9.
description
6.
Cohen, Bruce H.
"The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders."
Methods
51.4 (2010): 364-373.
description
7.
Pfeffer, G.
"Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations."
Neurology
81.24 (2013): 2073-2081.
description
8.
Finlayson, S.
"Congenital myasthenic syndromes: an update."
Practical neurology
13.2 (2013): 80-91.
description
9.
Kinghorn, K J.
"Hypertrophic olivary degeneration on magnetic resonance imaging in mitochondrial syndromes associated with POLG and SURF1 mutations."
Journal of neurology
260.1 (2012): 3-9.
description
10.
Hinnell, C.
"Dystonia in mitochondrial spinocerebellar ataxia and epilepsy syndrome associated with novel recessive POLG mutations."
Movement disorders
27.1 (2012): 162-163.
description
11.
Ringel, R.
"Structure of human mitochondrial RNA polymerase."
Nature
478.7368 (2011): 269-273.
description
12.
Milone, M.
"Novel POLG splice site mutation and optic atrophy."
Archives of neurology
68.6 (2011): 806-11.
description
13.
Isohanni, P.
"POLG1 manifestations in childhood."
Neurology
76.9 (2011): 811-815.
description
14.
Schls, L.
"POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe."
Movement disorders
25.15 (2010): 2678-2682.
description
15.
Magner, M.
"Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures."
European journal of paediatric neurology
15.2 (2010): 101-108.
description
16.
Morava, E.
"Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defective oxidative phosphorylation in two siblings with Sengers-like syndrome."
European journal of pediatrics
163.8 (2004): 467-71.
description
17.
Tzoulis, C.
"Melas associated with mutations in the polg1 gene."
Neurology
70.13 (2008): 1054-5.
description
18.
Shadel, G.
"Mitochondrial DNA maintenance in vertebrates."
Annual Review of Biochemistry
66.1 (1997): 409-435.
description
19.
Hakonen, H.
"Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European founders."
European journal of human genetics
15.7 (2007): 779-783.
description
20.
Caballero, Pedro Enrique Jiménez E.
"Chronic progressive external ophthalmoplegia: a report of 6 cases and a review of the literature."
The Neurologist
13.1 (2006): 33-6.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
ProCite
Reference Manager
EndNote
RefWorks
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Humble, M M
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Humble, M M
last name
initials
Other articles by this author? -- using
Web of Science
author:
Humble, M M
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.