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Description
Hypophosphatasia Autosomal dominant or autosomal recessive rare metabolic disease with an extraordinary range of severity caused by loss-of-function mutations within ALPL , which encodes TNALP

Items described in this study will be made available to the scientific community by contacting M.G.J

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doi: 10.18632/oncotarget.13523 194 ArranzADoxakiCVergadiEMartinez de la TorreYVaporidiKLagoudakiEDet al
