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Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin.
Imtiaz, Faiqa; Rashed, Mohamed S; Al-Mubarak, Bashayer; Allam, Rabab; El-Karaksy, Hanaa; Al-Hassnan, Zuhair; Al-Owain, Mohammed; Al-Zaidan, Hamad; Rahbeeni, Zuhair; Qari, Alya; Meyer, Brian F; Al-Sayed, Moeen.
Affiliation
  • Imtiaz F; Department of Genetics, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia. fahmad@kfshrc.edu.sa
Mol Genet Metab ; 104(4): 688-90, 2011 Dec.
Article in En | MEDLINE | ID: mdl-21764616
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tyrosinemias / Hydrolases / Mutation Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Country/Region as subject: Africa / Asia Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2011 Type: Article Affiliation country: Saudi Arabia
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tyrosinemias / Hydrolases / Mutation Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Country/Region as subject: Africa / Asia Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2011 Type: Article Affiliation country: Saudi Arabia