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Rapidly progressive case of Alpers disease with a rare POLG1 mutation.

Authors :
McCoy B
Rowley R
Ryan S
Lynch B
King M
Farrell MA
Source :
Developmental Medicine & Child Neurology; Jan2007 Supplement 108, Vol. 49, p29-29, 1p
Publication Year :
2007

Details

Language :
English
ISSN :
00121622
Volume :
49
Database :
Complementary Index
Journal :
Developmental Medicine & Child Neurology
Publication Type :
Academic Journal
Accession number :
105545694

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