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1دورية أكاديمية
المؤلفون: Bidchol AM; Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India., Dalal A, Shah H, S S, Nampoothiri S, Kabra M, Gupta N, Danda S, Gowrishankar K, Phadke SR, Kapoor S, Kamate M, Verma IC, Puri RD, Sankar VH, Devi AR, Patil SJ, Ranganath P, Jain SJ, Agarwal M, Singh A, Mishra P, Tamhankar PM, Gopinath PM, Nagarajaram HA, Satyamoorthy K, Girisha KM
المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2014 Nov; Vol. 164A (11), pp. 2793-801. Date of Electronic Publication: 2014 Sep 22.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
مواضيع طبية MeSH: Mutation*, Chondroitinsulfatases/*genetics , Mucopolysaccharidosis IV/*genetics , White People/*genetics, Adolescent ; Adult ; Alleles ; Amino Acid Substitution ; Child ; Child, Preschool ; Chondroitinsulfatases/metabolism ; Computational Biology ; DNA Mutational Analysis ; Enzyme Activation ; Female ; Gene Frequency ; Gene Order ; Humans ; India ; Infant ; Male ; Mucopolysaccharidosis IV/diagnosis ; Polymorphism, Single Nucleotide ; Pregnancy ; Prenatal Diagnosis ; Young Adult
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2دورية أكاديمية
المؤلفون: Phani NM; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Guddattu V; Department of Statistics, Manipal University, Manipal, Karnataka, India., Bellampalli R; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Seenappa V; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Adhikari P; Department of Medicine, Kasturba Medical College, Manipal University, Mangalore, Karnataka, India., Nagri SK; Department of Medicine, Kasturba Medical College, Manipal University, Manipal, Karnataka, India., D Souza SC; Department of Medicine, Kasturba Medical College, Manipal University, Mangalore, Karnataka, India., Mundyat GP; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Satyamoorthy K; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Rai PS; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India.
المصدر: PloS one [PLoS One] 2014 Sep 23; Vol. 9 (9), pp. e107021. Date of Electronic Publication: 2014 Sep 23 (Print Publication: 2014).
نوع المنشور: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review; Systematic Review
بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
مواضيع طبية MeSH: Asian People/*genetics , Diabetes Mellitus, Type 2/*ethnology , Diabetes Mellitus, Type 2/*genetics , Potassium Channels, Inwardly Rectifying/*genetics , White People/*genetics, Adult ; Aged ; Case-Control Studies ; DNA Copy Number Variations ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genetic Variation ; Humans ; India ; Middle Aged ; Polymorphism, Single Nucleotide