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Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening

✍ Scribed by Jaffar Alfardan; Al-Walid Mohsen; Sara Copeland; Jay Ellison; Laura Keppen-Davis; Marianne Rohrbach; Berkley R. Powell; Jane Gillis; Dietrich Matern; Jeffrey Kant; Jerry Vockley


Book ID
116989003
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
573 KB
Volume
100
Category
Article
ISSN
1096-7192

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