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Published Erratum
. 2019 Sep;91(3):471-473.
doi: 10.1111/cen.14068.

Erratum

No authors listed
Published Erratum

Erratum

No authors listed. Clin Endocrinol (Oxf). 2019 Sep.
No abstract available

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Erratum for

References

REFERENCES

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    1. Shabir I, Khurana ML, Joseph AA, et al. Phenotype, genotype and gender identity in a large cohort of patients from India with 5α-reductase 2 deficiency. Andrology. 2015;3(6):1132-1139.
    1. Veiga-Junior NN, Medaets PA, Petroli RJ, et al. Clinical and laboratorial features that may differentiate 46,XY DSD due to partial androgen insensitivity and 5α-reductase type 2 deficiency. Int J Endocrinol. 2012;2012:964876.
    1. Zhu H, Liu W, Han B, et al. Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiency. Clin Endocrinol (Oxf). 2014;81(5):711-720.
    1. Maimoun L, Philibert P, Cammas B, et al. Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients. J Clin Endocrinol Metab. 2011;96(2):296-307.

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