Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia (Q29147393)

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Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia
scientific journal article

    Statements

    title
    Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia (English)
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    author name string
    Yoko A. Ito
    series ordinal
    1
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    Tim K. Footz
    series ordinal
    2
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    Fred B. Berry
    series ordinal
    3
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    Farideh Mirzayans
    series ordinal
    4
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    May Yu
    series ordinal
    5
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    Arif O. Khan
    series ordinal
    6
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    Michael A. Walter
    series ordinal
    7
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    publication date
    1 August 2009
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    volume
    50
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    page(s)
    3573–3579
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017
    issue
    8
    1 reference
    stated in
    PubMed
    PubMed ID
    19279310
    retrieved
    4 April 2017

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                      Retrieved from "https://www.wikidata.org/w/index.php?title=Q29147393&oldid=1786009308"