Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL gene.

Spentchian, M; Merrien, Y; Herasse, M; Dobbie, Z; Gläser, D; Holder, S E; Ivarsson, S-A; Kostiner, D; Mansour, S; Norman, A; Roth, J; Stipoljev, F; Taillemite, J-L; van der Smagt, J J; Serre, J-L; Simon-Bouy, B; Taillandier, A; Mornet, E

Spentchian, M; Merrien, Y; Herasse, M; Dobbie, Z; Gläser, D; Holder, S E; Ivarsson, S-A; Kostiner, D; Mansour, S; Norman, A; Roth, J; Stipoljev, F; Taillemite, J-L; van der Smagt, J J; Serre, J-L; Simon-Bouy, B; Taillandier, A; Mornet, E.

Affiliation

Spentchian M; Centre d'Etudes de Biologie Prénatal-SESEP, Université de Versailles-Saint Quentin en Yvelines, Versailles, France.

Hum Mutat ; 22(1): 105-6, 2003 Jul.

Article in En | MEDLINE | ID: mdl-12815606

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Collection: 01-internacional Database: MEDLINE Main subject: Alkaline Phosphatase / Hypophosphatasia / Mutation Type of study: Clinical_trials / Diagnostic_studies Limits: Female / Humans / Male / Newborn / Pregnancy Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2003 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos

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