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A neonatal-onset succinyl-CoA:3-ketoacid CoA transferase (SCOT)-deficient patient with T435N and c.658-666dupAACGTGATT p.N220_I222dup mutations in theOXCT1gene

✍ Scribed by Fukao, Toshiyuki; Ishii, Tomohiro; Amano, Naoko; Kursula, Petri; Takayanagi, Masaki; Murase, Keiko; Sakaguchi, Naomi; Kondo, Naomi; Hasegawa, Tomonobu


Book ID
125356667
Publisher
Springer
Year
2010
Tongue
English
Weight
374 KB
Volume
33
Category
Article
ISSN
0141-8955

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