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Tiina Robins

Department of Molecular Medicine and Surgery

Center for Molecular Medicine (CMM) L8:02

Karolinska Institutet/Karolinska University Hospital

17176

Sweden

[email]@ki.se

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Affiliation

Department of Molecular Medicine and Surgery, Center for Molecular Medicine (CMM) L8:02, Karolinska Institutet/Karolinska University Hospital, 17176, Sweden. 2006 - 2007

References

Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia. Robins, T., Bellanne-Chantelot, C., Barbaro, M., Cabrol, S., Wedell, A., Lajic, S. J. Mol. Med. (2007) [Pubmed]
Molecular model of human CYP21 based on mammalian CYP2C5: structural features correlate with clinical severity of mutations causing congenital adrenal hyperplasia. Robins, T., Carlsson, J., Sunnerhagen, M., Wedell, A., Persson, B. Mol. Endocrinol. (2006) [Pubmed]