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Clinical and genetic analysis of a Korean patient with Fukuyama congenital muscular dystrophy

โœ Scribed by Jeehun Lee; Bo Lyun Lee; Munhyang Lee; Ji Hye Kim; Jong-Won Kim; Chang-Seok Ki


Book ID
119303339
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
275 KB
Volume
281
Category
Article
ISSN
0022-510X

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โœ Yoshioka, Mieko ;Kuroki, Shigekazu ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 503 KB

The association of congenital muscular dystrophy (CMD) with type I1 lissencephaly and ocular anomalies is found in Fukuyama CMD (FCMD), the Walker-Warburg syndrome (WWS), and muscle-eye-brain disease (MEBD). The classification of these disorders remains controversial. Between 1972 and 1992, we perfo