Mutation analysis on confirmed cases of 2-methylbutyryl Co-A dehydrogenase (SBCAD) deficiency in Hmong infants identified by newborn screening using tandem mass spectrometry.
Author(s):
Baker, M. W.; Van Calcar, S. C.; Litsheim, T.; Hoffman, G.; Vockley, J.; Rhead, W. J.; Wolff, J. A.; Durkin, M. S.
Format:
Journal article
Citation:
Molecular Genetics And Metabolism, Volume 90, Issue 3 (2007-03). pp. 246-246.