| dc.contributor.author | Lin, Z | en_US |
| dc.contributor.author | Zhao, J | en_US |
| dc.contributor.author | Nitoiu, D | en_US |
| dc.contributor.author | Scott, CA | en_US |
| dc.contributor.author | Plagnol, V | en_US |
| dc.contributor.author | Smith, FJD | en_US |
| dc.contributor.author | Wilson, NJ | en_US |
| dc.contributor.author | Cole, C | en_US |
| dc.contributor.author | Schwartz, ME | en_US |
| dc.contributor.author | McLean, WHI | en_US |
| dc.contributor.author | Wang, H | en_US |
| dc.contributor.author | Feng, C | en_US |
| dc.contributor.author | Duo, L | en_US |
| dc.contributor.author | Zhou, EY | en_US |
| dc.contributor.author | Ren, Y | en_US |
| dc.contributor.author | Dai, L | en_US |
| dc.contributor.author | Chen, Y | en_US |
| dc.contributor.author | Zhang, J | en_US |
| dc.contributor.author | Xu, X | en_US |
| dc.contributor.author | O'Toole, EA | en_US |
| dc.contributor.author | Kelsell, DP | en_US |
| dc.contributor.author | Yang, Y | en_US |
| dc.date.accessioned | 2017-06-12T08:40:09Z | |
| dc.date.available | 2014-12-30 | en_US |
| dc.date.issued | 2015-03-05 | en_US |
| dc.date.submitted | 2017-03-20T14:23:50.996Z | |
| dc.identifier.issn | 0002-9297 | en_US |
| dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/23763 | |
| dc.description.sponsorship | This work was
supported in part by China National Funds for Distinguished
Young Scientists (81425020 to Y.Y.), National Natural Science
Foundation of China (81271744 to Y.Y. and 81201220 to Z.L.), Beijing
Higher Education Young Elite Teacher Project (YETP0069
for Z.L.), and Shenzhen Key Laboratory of Cognitive Genomics
(CXB201108250094A). F.J.D.S. and N.J.W. are supported by grants
from the Pachyonychia Congenita Project. The Centre for Dermatology
and Genetic Medicine at the University of Dundee is supported
by a Wellcome Trust Strategic Award (098439/Z/12/Z to
W.H.I.M.). This study is also funded, in part, by Barts and the London
Charity (D.P.K.). | en_US |
| dc.format.extent | 440 - 447 | en_US |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | AMERICAN JOURNAL OF HUMAN GENETICS | en_US |
| dc.title | Loss-of-Function Mutations in CAST Cause Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle Pads | en_US |
| dc.type | Article | |
| dc.identifier.doi | 10.1016/j.ajhg.2014.12.026 | en_US |
| pubs.author-url | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000350747800016&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
| pubs.issue | 3 | en_US |
| pubs.notes | Not known | en_US |
| pubs.publication-status | Published | en_US |
| pubs.volume | 96 | en_US |
