Rare Disease Report

Alport Syndrome Foundation - Its Past, Present, and Future

OCTOBER 31, 2015
Sharon Lagas

Sharon Lagas, president of the Alport Syndrome Foundation talks about the history of the foundation, resources for Alport syndrome patients and upcoming Kidney Week plans at the at 2015 NORD Breakthrough Summit.

For more information, visit http://alportsyndrome.org.

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