Molecular basis of perinatal hypophosphatasia with tissue-nonspecific alkaline phosphatase bearing a conservative replacement of valine by alanine at position 406. Structural importance of the crown domain.
about
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.Molecular defect of tissue-nonspecific alkaline phosphatase bearing a substitution at position 426 associated with hypophosphatasia.Glycosylation-deficient mutations in tissue-nonspecific alkaline phosphatase impair its structure and function and are linked to infantile hypophosphatasia.A dimerization defect caused by a glycine substitution at position 420 by serine in tissue-nonspecific alkaline phosphatase associated with perinatal hypophosphatasia.
P2860
Molecular basis of perinatal hypophosphatasia with tissue-nonspecific alkaline phosphatase bearing a conservative replacement of valine by alanine at position 406. Structural importance of the crown domain.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
@zh-hans
2008年学术文章
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2008年学术文章
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2008年學術文章
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2008年學術文章
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name
Molecular basis of perinatal h ...... mportance of the crown domain.
@en
Molecular basis of perinatal h ...... mportance of the crown domain.
@nl
type
label
Molecular basis of perinatal h ...... mportance of the crown domain.
@en
Molecular basis of perinatal h ...... mportance of the crown domain.
@nl
prefLabel
Molecular basis of perinatal h ...... mportance of the crown domain.
@en
Molecular basis of perinatal h ...... mportance of the crown domain.
@nl
P2093
P2860
P1433
P1476
Molecular basis of perinatal h ...... mportance of the crown domain.
@en
P2093
Kimimitsu Oda
Makiko Nasu
Miwa Sohda
Natsuko Numa
Tadashi Noda
Yoko Ishida
Yoshio Misumi
P2860
P304
P356
10.1111/J.1742-4658.2008.06414.X
P407
P577
2008-04-18T00:00:00Z