An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity (Q28202722)

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scientific article (publication date: June 2002)
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An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity
scientific article (publication date: June 2002)

    Statements

    An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity (English)
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    Yvonne Lundberg Giwercman
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    Agneta Nordenskjöld
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    E Martin Ritzén
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    Karl Olof Nilsson
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    Sten-A Ivarsson
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    Ulla Grandell
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    Anna Wedell
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    June 2002
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    87
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    6
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    2623-8
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