A sequence variation in 3'UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia (Q56982423)

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L Baldazzi

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M Barbaro

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A Nicoletti

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V Conti

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P Pirazzoli

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A Wedell

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A Cicognani

Journal of Endocrinological Investigation

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language of work or name

English

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publication date

March 2012

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published in

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volume

35

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issue

3

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page(s)

298-305

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exact match

https://scigraph.springernature.com/pub.10.3275/7680

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Mutational spectrum of congenital adrenal hyperplasia in Slovenian patients: a novel Ala15Thr mutation and Pro30Leu within a larger gene conversion associated with a severe form of the disease.

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