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European Journal of Medical Genetics|June 11, 2022
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular diseaseAnett Marais, Aida M Bertoli-Avella, Christian Beetz, et al.
Pediatric Neurology|July 16, 2022
Hereditary Hyperekplexia in Saudi ArabiaAmal Aldhilan, Afnan Alhakeem, Sumayah Al Hajjaj, et al.
JACC. Advances|August 6, 2026
The Gulf Chronic Total Occlusion Registry: Short- and Long-Term Outcomes Across Management StrategiesAmin Daoulah, Mokhtar Abdirahman Kahin, Prashanth Panduranga, et al.
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