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Biotin-sensitive 3-methylcrotonylglycinuria in a patient wit…
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay%2C ectodermal abnormalities%2C neonatal progeroid appearance%2C and developmental delay.
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay%2C ectodermal abnormalities%2C neonatal progeroid appearance%2C and developmental delay.
Article, Chapter
Authors: S. Koene
Publication: Clinical Dysmorphology, Volume:17, Issue:3, Page(s):195
Published: Lippincott Williams and Wilkins, Inc., 2008
ISSN: 0962-8827
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