Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations (Q37141446)

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scientific article published on August 1992
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English
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations
scientific article published on August 1992

    Statements

    Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations (English)
    1 reference
    A Wedell
    1 reference
    E M Ritzén
    1 reference
    B Haglund-Stengler
    1 reference
    H Luthman
    1 reference
    1 August 1992
    1 reference
    89
    1 reference
    15
    1 reference
    7232-7236
    1 reference

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