Double mutation (A171T) and (D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States
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G. Buck | B. Wolf | K. L. Swango | J. Hymes | K. Norrgard | R. Pomponio | T. Reynolds | Karen J. Norrgard | Robert J. Pomponio | Katie L. Swango