Mutations in the Lysyl Hydroxylase 1 Gene That Result in Enzyme Deficiency and the Clinical Phenotype of Ehlers–Danlos Syndrome Type VI
- 1 September 2000
- journal article
- review article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 71 (1-2) , 212-224
- https://doi.org/10.1006/mgme.2000.3076
Abstract
No abstract availableKeywords
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