Mutation of the Type X Collagen Gene (COL10A1) Causes Spondylometaphyseal Dysplasia
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference16 articles.
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3. Japanese type of spondylo-metaphyseal dysplasia;Hasegawa;Pediatr Radiol,1994
4. Mutations in the N-terminal globular domain of the type X collagen gene (COL10A1) in patients with Schmid metaphyseal chondrodysplasia;Ikegawa;Hum Mutat,1997
5. Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition;Jacenko;Nature,1993
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