Enzyme Replacement Therapy for Murine Hypophosphatasia

INTRODUCTION: Hypophosphatasia (HPP) is the inborn error of metabolism that features rickets or osteomalacia caused by loss-of-function mutation(s) within the gene that encodes the tissue-nonspecific isozyme of alkaline phosphatase (TNALP). Consequently, natural substrates for this ectoenzyme accumu...

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Detalhes bibliográficos
Main Authors: Millán, José Luis, Narisawa, Sonoko, Lemire, Isabelle, Loisel, Thomas P, Boileau, Guy, Leonard, Pierre, Gramatikova, Svetlana, Terkeltaub, Robert, Camacho, Nancy Pleshko, McKee, Marc D, Crine, Philippe, Whyte, Michael P
Formato: Artigo
Idioma:Inglês
Publicado em: Amer Soc Bone & Mineral Res. 2008
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2652241/
https://ncbi.nlm.nih.gov/pubmed/18086009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1359/JBMR.071213
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