A Novel Nonstop Mutation in the Stop Codon and a Novel Missense Mutation in the Type II 3 -Hydroxysteroid Dehydrogenase (3 -HSD) Gene Causing, Respectively, Nonclassic and Classic 3 -HSD Deficiency Congenital Adrenal Hyperplasia (Q55885446)

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A Novel Nonstop Mutation in the Stop Codon and a Novel Missense Mutation in the Type II 3 -Hydroxysteroid Dehydrogenase (3 -HSD) Gene Causing, Respectively, Nonclassic and Classic 3 -HSD Deficiency Congenital Adrenal Hyperplasia
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    Statements

    A Novel Nonstop Mutation in the Stop Codon and a Novel Missense Mutation in the Type II 3 -Hydroxysteroid Dehydrogenase (3 -HSD) Gene Causing, Respectively, Nonclassic and Classic 3 -HSD Deficiency Congenital Adrenal Hyperplasia (English)
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    S. Pang
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    1 June 2002
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    87
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    6
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    2556-2563
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