Abstract
Homocystinuria is an autosomal recessive inherited enzymatic defect of methionine metabolism that is characterised by cystathionine β-synthetase deficiency.
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© 2009 Springer-Verlag/Wien
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(2009). Homocystinuria. In: Rovenský, J., Payer, J. (eds) Dictionary of Rheumatology. Springer, Vienna. https://doi.org/10.1007/978-3-211-79280-3_441
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DOI: https://doi.org/10.1007/978-3-211-79280-3_441
Publisher Name: Springer, Vienna
Print ISBN: 978-3-211-68584-6
Online ISBN: 978-3-211-79280-3
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