Wrn Mutations in Werner Syndrome Patients: Genomic Rearrangements, Unusual Intronic Mutations and Ethnic-Specific Alterations

AuthID
P-003-58C
29
Author(s)
Lee, L
·
Nuernberg, G
·
Saha, B
·
Nuernberg, P
·
[+4]·
[+3]·
[+2]·
Poot, M
·
Ippel, PF
·
Hoehn, H
·
Martin, GM
·
Kubisch, C
·
Oshima, J
Document Type
Article
Year published
2010
Published
in HUMAN GENETICS, ISSN: 0340-6717
Volume: 128, Issue: 1, Pages: 103-111 (9)
Indexing
Publication Identifiers
Pubmed: 20443122
Scopus: 2-s2.0-77954025436
Wos: WOS:000278737600009
Source Identifiers
ISSN: 0340-6717
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Name Order Name   Name Order Name   Name Order Name
1 Friedrich, K;   2 Lee, L;   3 Leistritz, DF;
4 Nuernberg, G;   5 Saha, B;   6 Hisama, FM;
7 Eyman, DK;   8 Lessel, D;   9 Nuernberg, P;
10 Li, CM;   11 Garcia F Villalta, MJ;   12 Kets, CM;
13 Schmidtke, J;   14 Cruz, VT ;   15 Van den Akker, PC;
16 Boak, J;   17 Peter, D;   18 Compoginis, G;
19 Cefle, K;   20 Ozturk, S;   21 Lopez, N;
22 Wessel, T;   23 Poot, M;   24 Ippel, PF;
25 Groff Kellermann, B;   26 Hoehn, H;   27 Martin, GM;
28 Kubisch, C;   29 Oshima, J;