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Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus

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


Book ID
109110745
Publisher
Wiley (Blackwell Publishing)
Year
2008
Tongue
English
Weight
242 KB
Volume
49
Category
Article
ISSN
0013-9580

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