دورية أكاديمية

Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia

التفاصيل البيبلوغرافية
العنوان: Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia
المؤلفون: Dave A., Laurie K., Staffieri S.E., Taranath D., Mackey D.A., Mitchell P., Wang J.J., Craig J.E., Burdon K.P., Sharma S.
المساهمون: DUKE-NUS MEDICAL SCHOOL
المصدر: Unpaywall 20191101
سنة النشر: 2013
المجموعة: National University of Singapore: ScholarBank@NUS
مصطلحات موضوعية: ephrin A1, ephrin A5, article, Australia, autophosphorylation, congenital cataract, EPHA2 gene, exome, exon, family history, gene, gene mutation, gene sequence, genetic disorder, genetic screening, genetic variability, haplotype, human, microsatellite marker, missense mutation, phenotype, population research, protein domain, protein motif, protein phosphorylation, protein protein interaction, sequence alignment, sequence analysis, signal transduction, single nucleotide polymorphism
الوصف: 10.1371/journal.pone.0072518 ; PLoS ONE ; 8 ; 8 ; e72518
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 19326203
العلاقة: Dave A., Laurie K., Staffieri S.E., Taranath D., Mackey D.A., Mitchell P., Wang J.J., Craig J.E., Burdon K.P., Sharma S. (2013). Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia. PLoS ONE 8 (8) : e72518. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0072518Test; https://scholarbank.nus.edu.sg/handle/10635/161273Test
الإتاحة: https://doi.org/10.1371/journal.pone.0072518Test
https://scholarbank.nus.edu.sg/handle/10635/161273Test
حقوق: Attribution 4.0 International ; http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.36A37C7C
قاعدة البيانات: BASE