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Year | Number of Results |
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1998 | 1 |
2003 | 1 |
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Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II.
Eur J Pediatr. 1998 May;157(5):378-81. doi: 10.1007/s004310050833.
Eur J Pediatr. 1998.
PMID: 9625333
A compound heterozygote case of type II aldosterone synthase deficiency.
Dunlop FM, Crock PA, Montalto J, Funder JW, Curnow KM.
Dunlop FM, et al.
J Clin Endocrinol Metab. 2003 Jun;88(6):2518-26. doi: 10.1210/jc.2003-030353.
J Clin Endocrinol Metab. 2003.
PMID: 12788848
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Aldosterone synthase deficiency type II with hypospadias.
Gucev Z, Tasic V, Pop-Jordanova N, Riepe FG.
Gucev Z, et al.
Indian Pediatr. 2012 Apr;49(4):318-20.
Indian Pediatr. 2012.
PMID: 22565077
Free article.
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Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II.
Jessen CL, Christensen JH, Birkebaek NH, Rittig S.
Jessen CL, et al.
Acta Paediatr. 2012 Nov;101(11):e519-25. doi: 10.1111/j.1651-2227.2012.02823.x.
Acta Paediatr. 2012.
PMID: 22931312
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Fission yeast Schizosaccharomyces pombe as a new system for the investigation of corticosterone methyloxidase deficiency-causing mutations.
Tin MK, Hakki T, Bernhardt R.
Tin MK, et al.
J Steroid Biochem Mol Biol. 2011 Mar;124(1-2):31-7. doi: 10.1016/j.jsbmb.2011.01.002. Epub 2011 Jan 13.
J Steroid Biochem Mol Biol. 2011.
PMID: 21237269
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