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Congenital glaucoma and CYP1B1: an old story revisited.
Alsaif, Hessa S; Khan, Arif O; Patel, Nisha; Alkuraya, Hisham; Hashem, Mais; Abdulwahab, Firdous; Ibrahim, Niema; Aldahmesh, Mohammed A; Alkuraya, Fowzan S.
Afiliación
  • Alsaif HS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Khan AO; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Patel N; Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
  • Alkuraya H; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Hashem M; Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
  • Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Aldahmesh MA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hum Genet ; 138(8-9): 1043-1049, 2019 Sep.
Article en En | MEDLINE | ID: mdl-29556725

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glaucoma / Citocromo P-450 CYP1B1 Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Hum Genet Año: 2019 Tipo del documento: Article País de afiliación: Arabia Saudita

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glaucoma / Citocromo P-450 CYP1B1 Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Hum Genet Año: 2019 Tipo del documento: Article País de afiliación: Arabia Saudita