(Q55933562)

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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

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title

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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main subject

congenital adrenal hyperplasia

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Y. L. Giwercman

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language of work or name

English

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publication date

1 June 2002

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published in

The Journal of Clinical Endocrinology and Metabolism

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volume

87

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issue

6

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page(s)

2623-2628

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DOI

10.1210/JC.87.6.2623

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(Q55933562)

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

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