Dopamine β-Hydroxylase Deficiency Associated with Mutations in a Copper Transporter Gene
- 1 January 1997
- book chapter
- Published by Elsevier
- Vol. 42, 66-68
- https://doi.org/10.1016/s1054-3589(08)60697-3
Abstract
No abstract availableKeywords
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- Predictive value of plasma catecholamine levels in neonatal detection of Menkes diseaseJournal of Inherited Metabolic Disease, 1993
- Plasma and cerebrospinal fluid neurochemical pattern in Menkes diseaseAnnals of Neurology, 1993
- Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPaseNature Genetics, 1993