Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature

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ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome

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Mendelian Disorder, Genetic Disorder, Genetics +4

Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains

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Expression Analysis, Protein Function, Protein Expression +8