Identification of a New Vhl Exon and Complex Splicing Alterations in Familial Erythrocytosis or Von Hippel-Lindau Disease

AuthID
P-00P-DEG
Document Type
Article
Year published
2018
Published
in BLOOD, ISSN: 0006-4971
Volume: 132, Issue: 5, Pages: 469-483 (15)
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Publication Identifiers
Scopus: 2-s2.0-85051219558
Wos: WOS:000440575800007
Source Identifiers
ISSN: 0006-4971
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Name Order Name   Name Order Name   Name Order Name
1 Lenglet, M;   2 Robriquet, F;   3 Schwarz, K;
4 Camps, C;   5 Couturier, A;   6 Hoogewijs, D;
7 Buffet, A;   8 Knight, SJL;   9 Gad, S;
10 Couve, S;   11 Chesnel, F;   12 Pacault, M;
13 Lindenbaum, P;   14 Job, S;   15 Dumont, S;
16 Besnard, T;   17 Cornec, M;   18 Dreau, H;
19 Pentony, M;   20 Kvikstad, E;   21 Deveaux, S;
22 Burnichon, N;   23 Ferlicot, S;   24 Vilaine, M;
25 Mazzella, JM;   26 Airaud, F;   27 Garrec, C;
28 Heidet, L;   29 Irtan, S;   30 Mantadakis, E;
31 Bouchireb, K;   32 Debatin, KM;   33 Redon, R;
34 Bezieau, S;   35 Bressac de Paillerets, B;   36 Teh, BT;
37 Girodon, F;   38 Randi, ML;   39 Putti, MC;
40 Bours, V;   41 VanWijk, R;   42 Goethert, JR;
43 Kattamis, A;   44 Janin, N;   45 Bento, C;
46 Taylor, JC;   47 Arlot Bonnemains, Y;   48 Richard, S;
49 Gimenez Roqueplo, AP;   50 Cario, H;   51 Gardie, B;