Ochronotic osteoarthropathy in a mouse model of alkaptonuria, and its inhibition by nitisinone

Author:

Preston Andrew J,Keenan Craig M,Sutherland Hazel,Wilson Peter J,Wlodarski Brenda,Taylor Adam M,Williams Dominic P,Ranganath Lakshminarayan R,Gallagher James A,Jarvis Jonathan C

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

Reference27 articles.

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2. Garrod's Croonian Lectures (1908) and the charter ‘Inborn Errors of Metabolism’: albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008;Scriver;J Inherit Metab Dis,2008

3. The nature of the defect in tyrosine metabolism in alcaptonuria;La Du;J Biol Chem,1958

4. The molecular basis of alkaptonuria;Fernández-Cañón;Nat Genet,1996

5. An update on molecular genetics of Alkaptonuria (AKU);Zatkova;J Inherit Metab Dis,2011

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