p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency

Rita Menassa, Véronique Tardy, F Despert, Claire Bouvattier-Morel, Jacques Brossier, Maryse Cartigny, Yves Morel

The Journal of Clinical Endocrinology & Metabolism · 2008 · 37 citations · 22 references

Abstract

According to phenotype and functional studies, p.H62L is a mild mutation, responsible for a more severe phenotype when associated with another mild mutation. These data are important for patient management and genetic counseling.

References

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