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Disease Markers
Volume 27, Issue 1, Pages 7-12
http://dx.doi.org/10.3233/DMA-2009-0640

Peptide Bound Hypohydroxyprolinuria in Handigodu Disease: A Familial Syndrome of Spondylo Epi(meta)physeal Dysplasia

Mallikarjun Badadani,1 S. V. Suresh Babu,1 K. T. Shetty,1 and S. S. Agarwal2

1Department of Neurochemistry, National Institute of Mental Health and Neuro Sciences, Bangalore-560029, India
2Advanced Center for Treatment Research and Education in Cancer (ACTREC) Navi Mumbai, India

Received 29 September 2009; Accepted 29 September 2009

Copyright © 2009 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Mallikarjun Badadani, S. V. Suresh Babu, K. T. Shetty, and S. S. Agarwal, “Peptide Bound Hypohydroxyprolinuria in Handigodu Disease: A Familial Syndrome of Spondylo Epi(meta)physeal Dysplasia,” Disease Markers, vol. 27, no. 1, pp. 7-12, 2009. https://doi.org/10.3233/DMA-2009-0640.