Novel human pathological mutations. Gene symbol: ALPL. Disease: hypophosphatasia

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Bibliographic Details
Published in:Human genetics 2009-04, Vol.125 (3), p.334-334
Main Authors: Bertola, Francesca, Arosio, C, Casati, G, Piperno, A, Crosti, F, Colombo, C
Format: Article
Language:English
Subjects:
Alkaline Phosphatase - deficiency
Alkaline Phosphatase - genetics
Amino Acid Substitution
Codon - genetics
Female
Humans
Hypophosphatasia - embryology
Hypophosphatasia - enzymology
Hypophosphatasia - genetics
Infant, Newborn
Molecular Sequence Data
Mutation, Missense
Pregnancy
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ISSN:1432-1203