Hypophosphatasia: Identification of five novel missense mutations (G507A, G705A, A748G, T1155C, G1320A) in the tissue-nonspecific alkaline phosphatase gene among Japanese patients-Reference-Cited by-同舟云学术

Hypophosphatasia: Identification of five novel missense mutations (G507A, G705A, A748G, T1155C, G1320A) in the tissue-nonspecific alkaline phosphatase gene among Japanese patients

Published:1998 Issue:S1 Volume:11 Page:S263-S267
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Goseki-Sone Masae,Orimo Hideo,Iimura Tadahiro,Takagi Yuzo,Watanabe Hisashi,Taketa Kazuhisa,Sato Seiji,Mayanagi Hideaki,Shimada Takashi,Oida Shinichiro

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Immunological study on hypophosphatasia;Goseki (Sone);Clinica Chimica Acta,1990

2. Identification of bone-type alkaline phosphatase mRNA from human periodontal ligament cells;Goseki (Sone);J Dent Res,1995

3. AhomoallelicGly317» Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian Mennonites;Greenberg;Genomics,1993

4. Sequence and characterization of the human intestinal alkaline phosphatase;Henthorn;J Biol Chem,1988

5. Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia;Henthorn;Proc Natl Acad Sci USA,1992

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