The XLH Network was formed in November 1996 as an international volunteer group of people affected by or interested in XLH, or X-linked hypophosphatemia. The XLH Network provides members with up-to-date information on diagnosis, treatment and the very latest research. Through the F-HYPDRR mailing list, the XLH Network helps connect patients with clinicians and researchers as well as with each other.
Last updated on 02/09/2013
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