Homozygous W748S mutation in thePOLG1gene in patients with juvenile-onset Alpers syndrome and status epilepticus-Reference-Cited by-同舟云学术

Homozygous W748S mutation in thePOLG1gene in patients with juvenile-onset Alpers syndrome and status epilepticus

Published:2008-06 Issue:6 Volume:49 Page:1038-1045
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Uusimaa Johanna,Hinttala Reetta,Rantala Heikki,Päivärinta Markku,Herva Riitta,Röyttä Matias,Soini Heidi,Moilanen Jukka S.,Remes Anne M.,Hassinen Ilmo E.,Majamaa Kari

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2008.01544.x/fullpdf

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4. POLG mutations and Alpers syndrome;Davidzon;Ann Neurol,2005

5. Early-onset familial parkinsonism due to POLG mutations;Davidzon;Ann Neurol,2006

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