Case Report
Common mutation underlying primary hyperoxaluria type1 in three Indian children
Volume 22 | Issue 6 | November-December 2012
Disclaimer:
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.