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Mutation of ATF6 causes autosomal recessive achromatopsia.
Ansar, Muhammad; Santos-Cortez, Regie Lyn P; Saqib, Muhammad Arif Nadeem; Zulfiqar, Fareeha; Lee, Kwanghyuk; Ashraf, Naeem Mahmood; Ullah, Ehsan; Wang, Xin; Sajid, Sundus; Khan, Falak Sher; Amin-ud-Din, Muhammad; Smith, Joshua D; Shendure, Jay; Bamshad, Michael J; Nickerson, Deborah A; Hameed, Abdul; Riazuddin, Saima; Ahmed, Zubair M; Ahmad, Wasim; Leal, Suzanne M.
Affiliation
  • Ansar M; Department of Molecular and Human Genetics, Center for Statistical Genetics, Baylor College of Medicine, 1 Baylor Plaza 700D, Houston, TX, 77030, USA.
Hum Genet ; 134(9): 941-50, 2015 Sep.
Article in En | MEDLINE | ID: mdl-26063662
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Full text: 1 Database: MEDLINE Main subject: Color Vision Defects / Frameshift Mutation / Activating Transcription Factor 6 Type of study: Etiology_studies / Prognostic_studies Limits: Adolescent / Animals / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2015 Type: Article Affiliation country: United States
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Full text: 1 Database: MEDLINE Main subject: Color Vision Defects / Frameshift Mutation / Activating Transcription Factor 6 Type of study: Etiology_studies / Prognostic_studies Limits: Adolescent / Animals / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2015 Type: Article Affiliation country: United States