Variable phenotype of a null PPP1R13L allele in children with dilated cardiomyopathy.

Autor: Tulbah S; Cardiovascular Genetics Program, Department of Translational Genomics, Center for Genomic Medicine, Riyadh, Saudi Arabia., Alruwaili N; Heart Center, King Faisal Specialist Hospital & Research Centre (KFSH&RC), Riyadh, Saudi Arabia., Alhashem A; Division of Medical Genetics, Department of Pediatrics, Prince Sultan Medical Military City, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Aljohany A; King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia., Alhadeq F; Cardiovascular Genetics Program, Department of Translational Genomics, Center for Genomic Medicine, Riyadh, Saudi Arabia., Brotons DCA; Heart Center, King Faisal Specialist Hospital & Research Centre (KFSH&RC), Riyadh, Saudi Arabia., Alwadai A; Heart Failure and Transplant Program, Prince Sultan Cardiac Center, Riyadh, Saudi Arabia., Al-Hassnan ZN; Cardiovascular Genetics Program, Department of Translational Genomics, Center for Genomic Medicine, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Jan; Vol. 194 (1), pp. 59-63. Date of Electronic Publication: 2023 Sep 12.