Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other (Q43213478)

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scientific article published on 22 December 2009
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English
Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other
scientific article published on 22 December 2009

    Statements

    Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other (English)
    Katja Dumic
    Robert Wilson
    Pavinee Thanasawat
    Zorana Grubic
    Vesna Kusec
    Maria I New
    22 December 2009
    891-894

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