Loss-Of-Function Mutations in Ptpn11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome

AuthID
P-002-SK2
28
Author(s)
Bowen, ME
·
Holm, IA
·
Campos Xavier, B
·
Bonafe, L
·
Ikegawa, S
·
[+2]·
[+1]·
[+1]·
[+1]·
[+1]·
[+2]·
Pedrini, E
·
Kasser, JR
·
Seidman, JG
·
Kurek, KC
·
Warman, ML
1
Editor(s)
Wilkie, Andrew O. M.
Document Type
Article
Year published
2011
Published
in PLOS GENETICS, ISSN: 1553-7390
Volume: 7, Issue: 4, Pages: e1002050 (11)
Indexing
Publication Identifiers
Pubmed: 21533187
Scopus: 2-s2.0-79955631529
Wos: WOS:000289977000031
Source Identifiers
ISSN: 1553-7390
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Name Order Name   Name Order Name   Name Order Name
1 Bowen, ME;   2 Boyden, ED;   3 Holm, IA;
4 Campos Xavier, B;   5 Bonafe, L;   6 Superti Furga, A;
7 Ikegawa, S;   8 Cormier Daire, V;   9 Bovee, JV;
10 Pansuriya, TC;   11 de Sousa, SB;   12 Savarirayan, R;
13 Andreucci, E;   14 Vikkula, M;   15 Garavelli, L;
16 Pottinger, C;   17 Ogino, T;   18 Sakai, A;
19 Regazzoni, BM;   20 Wuyts, W;   21 Sangiorgi, L;
22 Pedrini, E;   23 Zhu, M;   24 Kozakewich, HP;
25 Kasser, JR;   26 Seidman, JG;   27 Kurek, KC;
28 Warman, ML;