Cystathioninuria (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cystathioninuria" in English language version.

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doi.org

  • Wang, Jian; Hegele, Robert (April 2003). "Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)". Human Genetics. 112 (4): 404–8. doi:10.1007/s00439-003-0906-8. PMID 12574942. S2CID 37114507.
  • Scott, Ronald; Dassell, Steven; Clark, Sandra; Chiang-Teng, Cecilia; Swedberg, Kathryn (April 1970). "Cystathioninemia: A benign genetic condition". Journal of Pediatrics. 76 (4): 571–577. doi:10.1016/S0022-3476(70)80407-3. PMID 5420794.
  • Rajnerc, J.R.; Gennip, A.H.; Abeling, N.G.G.M.; van der Zee, J.M.; Voute, P.A. (1984). "Cystathioninuria in patients with neuroblastoma". Medical and Pediatric Oncology. 12 (2): 81–4. doi:10.1002/mpo.2950120203. PMID 6422219.
  • Pascal, Theresa; Gaull, Gerald; Beratis, Nicolas; Gillam, Bruce; Tallan, Harris (February 1978). "Cystathionase deficiency: evidence for genetic heterogeneity in primary cystathioninuria". Pediatric Research. 12 (2): 125–133. doi:10.1203/00006450-197802000-00012. PMID 417288.
  • Pascal, T.A.; Gaull, G.E.; Beratis, N.G.; Gillam, B.M.; Tallan, H.H.; Hirschhorn, K. (December 1975). "Vitamin B6-Responsive and Unresponsive Cystathioninuria: Two Variant Molecular Forms". Science. 190 (4220): 1209–11. Bibcode:1975Sci...190.1209P. doi:10.1126/science.1198108. PMID 1198108. S2CID 29035241.

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Wang, Jian; Hegele, Robert (April 2003). "Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)". Human Genetics. 112 (4): 404–8. doi:10.1007/s00439-003-0906-8. PMID 12574942. S2CID 37114507.
  • Scott, Ronald; Dassell, Steven; Clark, Sandra; Chiang-Teng, Cecilia; Swedberg, Kathryn (April 1970). "Cystathioninemia: A benign genetic condition". Journal of Pediatrics. 76 (4): 571–577. doi:10.1016/S0022-3476(70)80407-3. PMID 5420794.
  • Rajnerc, J.R.; Gennip, A.H.; Abeling, N.G.G.M.; van der Zee, J.M.; Voute, P.A. (1984). "Cystathioninuria in patients with neuroblastoma". Medical and Pediatric Oncology. 12 (2): 81–4. doi:10.1002/mpo.2950120203. PMID 6422219.
  • Pascal, Theresa; Gaull, Gerald; Beratis, Nicolas; Gillam, Bruce; Tallan, Harris (February 1978). "Cystathionase deficiency: evidence for genetic heterogeneity in primary cystathioninuria". Pediatric Research. 12 (2): 125–133. doi:10.1203/00006450-197802000-00012. PMID 417288.
  • Pascal, T.A.; Gaull, G.E.; Beratis, N.G.; Gillam, B.M.; Tallan, H.H.; Hirschhorn, K. (December 1975). "Vitamin B6-Responsive and Unresponsive Cystathioninuria: Two Variant Molecular Forms". Science. 190 (4220): 1209–11. Bibcode:1975Sci...190.1209P. doi:10.1126/science.1198108. PMID 1198108. S2CID 29035241.

rarediseases.info.nih.gov

omim.org

semanticscholar.org

api.semanticscholar.org

  • Wang, Jian; Hegele, Robert (April 2003). "Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)". Human Genetics. 112 (4): 404–8. doi:10.1007/s00439-003-0906-8. PMID 12574942. S2CID 37114507.
  • Pascal, T.A.; Gaull, G.E.; Beratis, N.G.; Gillam, B.M.; Tallan, H.H.; Hirschhorn, K. (December 1975). "Vitamin B6-Responsive and Unresponsive Cystathioninuria: Two Variant Molecular Forms". Science. 190 (4220): 1209–11. Bibcode:1975Sci...190.1209P. doi:10.1126/science.1198108. PMID 1198108. S2CID 29035241.