Associated Papers
Transmembrane Protein 43: Molecular and Pathogenetic Implications in Arrhythmogenic Cardiomyopathy and Various Other Diseases.
Orgil BO et al.
International Journal of Molecular Sciences, 2025
Postmortem Identification of Genetic Variations Associated with Sudden Unexpected Death in Young People.
Miura A et al.
International Heart Journal, 2024
Clinical and Genetic Features of Korean Inherited Arrhythmia Probands.
Jeong JH et al.
Korean Circulation Journal, 2023
37653714 (PubMed )
Supplement: kcj-53-693-s007.xls › kcj-53-693-s007
Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish.
Zink M et al.
International Journal of Molecular Sciences, 2022
Systems genetics analysis defines importance of TMEM43/LUMA for cardiac- and metabolic-related pathways.
Gu Q et al.
Physiological Genomics, 2022
Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death.
Ueda A et al.
Plos One, 2022
35486589 (PubMed )
Supplement: pone.0267751.s001.xls › SIDS3-full
Findings of a 1303 Korean whole-exome sequencing study.
Kwak SH et al.
Experimental & Molecular Medicine, 2017
28706299 (PubMed )
Supplement: emm2017142x4.xls › Table_S1
Fetal arrhythmogenic right ventricular cardiomyopathy with double mutations in TMEM43.
Honda T et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2016
TMEM43 mutations associated with arrhythmogenic right ventricular cardiomyopathy in non-Newfoundland populations.
Baskin B et al.
Human Genetics, 2013
TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
Liang WC et al.
Annals of Neurology, 2011
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