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A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations.
Parveen, Asia; Mirza, Muhammad U; Vanmeert, Michiel; Akhtar, Javed; Bashir, Hina; Khan, Saadullah; Shehzad, Saqib; Froeyen, Matheus; Ahmed, Wasim; Ansar, Muhammad; Wasif, Naveed.
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  • Parveen A; Institute of Molecular Biology and Biotechnology (IMBB), Centre for Research in Molecular Medicine (CRiMM), The University of Lahore, Lahore, Pakistan.
  • Mirza MU; Faculty of Life Sciences, University of Central Punjab (UCP), Lahore, Pakistan.
  • Vanmeert M; Department of Pharmaceutical Sciences, REGA Institute for Medical Research, Medicinal Chemistry, University of Leuven, Leuven, Belgium.
  • Akhtar J; Department of Pharmaceutical Sciences, REGA Institute for Medical Research, Medicinal Chemistry, University of Leuven, Leuven, Belgium.
  • Bashir H; Institute of Molecular Biology and Biotechnology (IMBB), Centre for Research in Molecular Medicine (CRiMM), The University of Lahore, Lahore, Pakistan.
  • Khan S; Institute of Molecular Biology and Biotechnology (IMBB), Centre for Research in Molecular Medicine (CRiMM), The University of Lahore, Lahore, Pakistan.
  • Shehzad S; Department of Biochemistry, Sharif Medical and Dental College, Lahore, Pakistan.
  • Froeyen M; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Pakistan.
  • Ahmed W; Faculty of Life Sciences, University of Central Punjab (UCP), Lahore, Pakistan.
  • Ansar M; Department of Pharmaceutical Sciences, REGA Institute for Medical Research, Medicinal Chemistry, University of Leuven, Leuven, Belgium.
  • Wasif N; Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Mol Genet Genomic Med ; 7(9): e902, 2019 09.
Article en En | MEDLINE | ID: mdl-31347285
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mutación Missense / Proteínas de Transporte de Catión / Simulación de Dinámica Molecular / Distrofias de Conos y Bastones / Amelogénesis Imperfecta Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article País de afiliación: Pakistán
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mutación Missense / Proteínas de Transporte de Catión / Simulación de Dinámica Molecular / Distrofias de Conos y Bastones / Amelogénesis Imperfecta Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article País de afiliación: Pakistán