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Functional Characterization of Two Novel Point Mutations in theCYP21Gene Causing Simple Virilizing Forms of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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Journal Title: | The Journal of Clinical Endocrinology & Metabolism |
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Authors and Corporations: | , , , , |
In: | The Journal of Clinical Endocrinology & Metabolism, 90, 2005, 1, p. 445-454 |
Type of Resource: | E-Article |
Language: | English |
published: |
The Endocrine Society
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Subjects: |