Kongenitale Nebennierenrindenhyperplasie (angeborenes adrenogenitales Syndrom) mit C21- und C11-Hydroxylase-Mangel
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-59043-6_21.pdf
Reference116 articles.
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3. Birnbaum MD, Rose LI (1984) Late onset adrenocortical hydroxylase deficiencies associated with menstrual dysfunction. Obstet Gynecol 63: 445–450
4. Bristow J, Gitelman SE, Tee MK, Staels B, Miller WL (1993) Abundant adrenal-specific transcription of the human P450c21A „pseudogene“. J Biol Chem 268: 12919–12924
5. Bristow J, Tee MK, Gitelman SE, Mellon SH, Miller WL (1993) Tenascin-X. A novel extracellular matrix protein encoded by the human XB gene overlapping P 450c21. J Cell Biol 122: 265–278
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