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Frequency of spinocerebellar ataxia types 1, 2, 3, 6, 7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia

โœ Scribed by Dong Kyu Jin; Myung Ryurl Oh; Seng Mi Song; Si Whan Koh; Munhyang Lee; Gyeong Moon Kim; Won-Yong Lee; Chin-San Chung; Kwang Ho Lee; Joo Hyuk Im; Myung Jong Lee; Jae Woo Kim; Myung Sik Lee


Publisher
Springer
Year
1999
Tongue
English
Weight
37 KB
Volume
246
Category
Article
ISSN
0340-5354

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โœ Brian M. Ross; Klaus Eder; Anna Moszczynska; Nikolaos Mamalias; Jacques Lamarche ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 175 KB ๐Ÿ‘ 2 views

Much evidence, derived from biochemical studies of both blood and autopsied brain, has suggested that phospholipid metabolism is abnormal in patients with Friedreich's ataxia (FA), a disorder characterized by severe neuronal loss in the spinal cord and lower brain stem with no, or only modest, damag