Conference
NEW GENES IN NEUROMUSCULAR DISEASES O.04 Heterozygous frameshift variants in hnRNPA2B1 cause a novel oculopharyngodistal muscular dystrophy
Authors
Mohassel P; Donkervoort S; Kim H; Foley A; Lornage X; Group HS; Foulds N; Hammans S; Haack T; Böhm J
Volume
30
Publisher
Elsevier
Publication Date
October 1, 2020
DOI
10.1016/j.nmd.2020.08.006
Conference proceedings
Neuromuscular Disorders
ISSN
0960-8966