Mapping genotype-phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome

Mohanasundaram, Kaavya A., Grover, Mani P., Crowley, Tamsyn, Goscinski, Andrzej and Wouters, Merridee 2017, Mapping genotype-phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome, Human mutation, vol. 38, no. 10, pp. 1378-1393, doi: 10.1002/humu.23252.

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Title Mapping genotype-phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome
Author(s) Mohanasundaram, Kaavya A.
Grover, Mani P.
Crowley, TamsynORCID iD for Crowley, Tamsyn orcid.org/0000-0002-3698-8917
Goscinski, Andrzej
Wouters, Merridee
Journal name Human mutation
Volume number 38
Issue number 10
Start page 1378
End page 1393
Total pages 16
Publisher John Wiley & Sons
Place of publication Chichester, Eng.
Publication date 2017-10
ISSN 1098-1004
Keyword(s) coiled-coil domain
complex diseases
disease mutations
lamin A
missense mutation
pleiotropy
point mutation
single-nucleotide polymorphisms
Language eng
DOI 10.1002/humu.23252
Field of Research 0604 Genetics
1103 Clinical Sciences
HERDC Research category C1 Refereed article in a scholarly journal
ERA Research output type C Journal article
Copyright notice ©2017, Wiley-Blackwell
Persistent URL http://hdl.handle.net/10536/DRO/DU:30098928

Document type: Journal Article
Collections: Faculty of Health
School of Medicine
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