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Mutations in the Lysyl Hydroxylase 1 Gene That Result in Enzyme Deficiency and the Clinical Phenotype of Ehlers–Danlos Syndrome Type VI

✍ Scribed by Heather N. Yeowell; Linda C. Walker

Book ID: 115639754
Publisher: Elsevier Science
Year: 2000
Tongue: English
Weight: 212 KB
Volume: 71
Category: Article
ISSN: 1096-7192
DOI: 10.1006/mgme.2000.3076

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