Biallelic Variants in the Transcription Factor Pax7 Are a New Genetic Cause of Myopathy

AuthID
P-00Q-MHQ
36
Author(s)
Feichtinger, RG
·
Makowski, C
·
Dort, J
·
Nguyen, TTM
·
[+1]·
[+2]·
[+1]·
[+12]·
Strom, TM
·
Mayr, JA
·
Schoels, L
·
Michaud, JL
·
Campeau, PM
·
Haack, TB
·
Dumont, NA
Document Type
Article
Year published
2019
Published
in GENETICS IN MEDICINE, ISSN: 1098-3600
Volume: 21, Issue: 11, Pages: 2521-2531 (11)
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-85065997521
Wos: WOS:000494989200016
Source Identifiers
ISSN: 1098-3600
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Name Order Name   Name Order Name   Name Order Name
1 Feichtinger, RG;   2 Mucha, BE;   3 Hengel, H;
4 Orfi, Z;   5 Makowski, C;   6 Dort, J;
7 D'Anjou, G;   8 Nguyen, TTM;   9 Buchert, R;
10 Juenger, H;   11 Freisinger, P;   12 Baumeister, S;
13 Schoser, B;   14 Ahting, U;   15 Keimer, R;
16 Nguyen, CTE;   17 Fabre, P;   18 Gauthier, J;
19 Miguet, M;   20 Lopes, F;   21 AlHakeem, A;
22 AlHashem, A;   23 Tabarki, B;   24 Kandaswamy, KK;
25 Bauer, P;   26 Steinbacher, P;   27 Prokisch, H;
28 Sturm, M;   29 Strom, TM;   30 Ellezam, B;
31 Mayr, JA;   32 Schoels, L;   33 Michaud, JL;
34 Campeau, PM;   35 Haack, TB;   36 Dumont, NA;