Biallelic C1Qbp Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies

AuthID
P-00N-3Y9
39
Author(s)
Feichtinger, RG
·
Kremer, LS
·
Yagi, M
·
Thompson, K
·
D'Souza, AR
·
[+19]·
Murayama, K
·
Ohtake, A
·
Rebelo Guiomar, P
·
Kohda, M
·
Kang, D
·
Mayr, JA
·
Taylor, RW
·
Okazaki, Y
·
Minczuk, M
·
Prokisch, H
Document Type
Article
Year published
2017
Published
in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297
Volume: 101, Issue: 4, Pages: 525-538 (14)
Indexing
Publication Identifiers
Wos: WOS:000412277300004
Source Identifiers
ISSN: 0002-9297
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Name Order Name   Name Order Name   Name Order Name
1 Feichtinger, RG;   2 Olahova, M;   3 Kishita, Y;
4 Garone, C;   5 Kremer, LS;   6 Yagi, M;
7 Uchiumi, T;   8 Jourdain, AA;   9 Thompson, K;
10 D'Souza, AR;   11 Kopajtich, R;   12 Alston, CL;
13 Koch, J;   14 Sperl, W;   15 Mastantuono, E;
16 Strom, TM;   17 Wortmann, SB;   18 Meitinger, T;
19 Pierre, G;   20 Chinnery, PF;   21 Chrzanowska Lightowlers, ZM;
22 Lightowlers, RN;   23 DiMauro, S;   24 Calvo, SE;
25 Mootha, VK;   26 Moggio, M;   27 Sciacco, M;
28 Comi, GP;   29 Ronchi, D;   30 Murayama, K;
31 Ohtake, A;   32 Rebelo Guiomar, P;   33 Kohda, M;
34 Kang, D;   35 Mayr, JA;   36 Taylor, RW;
37 Okazaki, Y;   38 Minczuk, M;   39 Prokisch, H;