Clinical utility gene card for: Xeroderma pigmentosum
Clinical utility gene card for: Xeroderma pigmentosum
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临床实用基因卡:着色性干皮病
DOI:
10.1038/ejhg.2013.233
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发表时间:
2014
影响因子:
5.2
通讯作者:
Emmert S
中科院分区:
文献类型:
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作者:
Schubert S;Lehmann J;Kalfon L;Slor H;Falik-Zaccai TC;Emmert S
1.5 Mutational spectrum XPA: 122 known disease-causing mutations from 101 patients. Mutations: 77 (63%) G> C, 3 (2%) T> A, and 2 (1.5%) G> T transversions, 30 (25%) transitions (20 of these are c. 682C> T stop codon mutations; GenBank accession number: NC_000009. 11), 8 (7%) deletions, and 2 (1.5%) insertions. Consequences: frameshifts, protein truncations, and functional relevant amino-acid substitutions. 1–3XPB/ERCC3: eight known disease-causing mutations from five patients. Mutations: 1 (12.5%) C> A transversion, 1 (12.5%) A> C transversion, 1 (12.5%) G> A transition, 3 (37, 5%) T> C transitions, 1 (12.5%) deletion (c. 807-808delT_T), and 1 (12.5%) insertion (c. 1421-1422insA). Consequences: two functional relevant amino-acid substitutions (c. 296T> C (p.(Phe99Ser)) and c. 355> C (p.(Thr199Pro))), and six frameshift/protein truncations (GenBank accession number: NC_000002. 11). 4 XPC: 51 known disease-causing mutations from 114 patients. Mutations: transitions, transversions, deletions, insertions, complex deletion/insertion mutations, and splice-site mutations. Consequences: frameshifts, protein truncations, and functional relevant amino-acid substitutions. Here, a phenotype correlation emerges indicating that XPC mutations only result in a classical XP
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DOI:
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发表时间:
2011
期刊:
影响因子:
--
作者:
J. Harper;A. Irvine;P. Hoeger;A. Yan
通讯作者:
A. Yan
DOI:
--
发表时间:
--
期刊:
影响因子:
--
作者:
通讯作者:
--
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
S. Emmert
通讯作者:
S. Emmert
影响因子:
3.6
作者:
A. Schäfer;L. Hofmann;A. Gratchev;P. Laspe;S. Schubert;A. Schürer;A. Ohlenbusch;M. Tzvetkov;C. Hallermann;J. Reichrath;M. P. Schön;S. Emmert
通讯作者:
S. Emmert
影响因子:
3.9
作者:
Oh, Kyu-Seon;Khan, Sikandar G.;Kraemer, Kenneth H.
通讯作者:
Kraemer, Kenneth H.