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Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutations

Crossref DOI link: https://doi.org/10.1007/s42000-018-0006-8

Published Online: 2018-04-16

Published Print: 2018-03

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Bulsari, Krupali

Maple-Brown, Louise

Falhammar, Henrik
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Text and Data Mining valid from 2018-03-01
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Article History

Received: 17 June 2017

Accepted: 30 November 2017

First Online: 16 April 2018

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: The authors declare that they have no conflict of interest.

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