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Kongenitale Nebennierenhyperplasie durch 17-alpha-Hydroxylase-Mangel (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kongenitale Nebennierenhyperplasie durch 17-alpha-Hydroxylase-Mangel" in German language version.

refsWebsite
Global rank German rank
2doi.org
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2nih.gov
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1orpha.net
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1omim.org
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1medscape.com
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doi.org

  • E. G. Biglieri, M. A. Herron, N. Brust: 17-hydroxylation deficiency in man. In: The Journal of clinical investigation. Band 45, Nummer 12, Dezember 1966, S. 1946–1954, doi:10.1172/JCI105499, PMID 4288776, PMC 292880 (freier Volltext).
  • V. Dhir, N. Reisch, C. M. Bleicken, J. Lebl, C. Kamrath, H. P. Schwarz, J. Grötzinger, W. G. Sippell, F. G. Riepe, W. Arlt, N. Krone: Steroid 17alpha-hydroxylase deficiency: functional characterization of four mutations (A174E, V178D, R440C, L465P) in the CYP17A1 gene. In: The Journal of clinical endocrinology and metabolism. Band 94, Nummer 8, August 2009, S. 3058–3064, doi:10.1210/jc.2009-0172, PMID 19454579.

medscape.com

emedicine.medscape.com

nih.gov

ncbi.nlm.nih.gov

  • E. G. Biglieri, M. A. Herron, N. Brust: 17-hydroxylation deficiency in man. In: The Journal of clinical investigation. Band 45, Nummer 12, Dezember 1966, S. 1946–1954, doi:10.1172/JCI105499, PMID 4288776, PMC 292880 (freier Volltext).
  • V. Dhir, N. Reisch, C. M. Bleicken, J. Lebl, C. Kamrath, H. P. Schwarz, J. Grötzinger, W. G. Sippell, F. G. Riepe, W. Arlt, N. Krone: Steroid 17alpha-hydroxylase deficiency: functional characterization of four mutations (A174E, V178D, R440C, L465P) in the CYP17A1 gene. In: The Journal of clinical endocrinology and metabolism. Band 94, Nummer 8, August 2009, S. 3058–3064, doi:10.1210/jc.2009-0172, PMID 19454579.

omim.org

orpha.net