A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene

Author:

Salo Antti M.,Cox Helen,Farndon Peter,Moss Celia,Grindulis Helen,Risteli Maija,Robins Simon P.,Myllylä Raili

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference29 articles.

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2. Hydroxylation of proline and lysine residues in collagen and other animal and plant proteins;Kivirikko,1992

3. Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3);Myllylä;J. Cell. Physiol.,2007

4. Primary structure, tissue distribution and chromosomal localization of a novel isoform of lysyl hydroxylase (lysyl hydroxylase 3);Valtavaara;J. Biol. Chem.,1998

5. Cloning and characterization of a third human lysyl hydroxylase isoform;Passoja;Proc. Natl. Acad. Sci. USA,1998

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