Mapping genotype–phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome
Version 2 2024-06-04, 02:37
Version 1 2017-10-01, 00:00
journal contribution
posted on 2024-06-04, 02:37 authored by KA Mohanasundaram, MP Grover, Tamsyn CrowleyTamsyn Crowley, Andrzej GoscinskiAndrzej Goscinski, MA WoutersMapping genotype–phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome
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United StatesLanguage
EnglishPublication classification
C Journal article, C1 Refereed article in a scholarly journalCopyright notice
2017, Wiley-BlackwellJournal
Human MutationVolume
38Pagination
1378-1393ISSN
1059-7794eISSN
1098-1004Issue
10Publisher
WILEYUsage metrics
Keywords
Science & TechnologyLife Sciences & BiomedicineGenetics & Hereditycoiled-coil domaincomplex diseasesdisease mutationslamin Amissense mutationpleiotropypoint mutationsingle-nucleotide polymorphismsSKIP RESIDUESMUTATIONSSUBSTITUTIONSEQUENCEDISEASESDATABASEFAMILYGENESROD3105 Genetics3102 Bioinformatics and computational biology
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