Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria (Q28270419)

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Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria
scientific article

    Statements

    title
    Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria (English)
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    author name string
    Barbara Kloeckener-Gruissem
    series ordinal
    1
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    Kristof Vandekerckhove
    series ordinal
    2
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    Gudrun Nürnberg
    series ordinal
    3
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    John Neidhardt
    series ordinal
    4
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    Christina Zeitz
    series ordinal
    5
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    Peter Nürnberg
    series ordinal
    6
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    Isaak Schipper
    series ordinal
    7
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    Wolfgang Berger
    series ordinal
    8
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    publication date
    March 2008
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    volume
    82
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    issue
    3
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    page(s)
    772-9
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    cites work

    Identifiers

     
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