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Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation
British Journal of Dermatology, 10/29/09
Schrander–Stumpel CTRM et al. – The authors speculate on the mechanism of dermal hypoplasia and resistance to PTH and suggest that subcutanous or dermal hypoplasia might be another feature which can be present in patients with AHO.
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