1. Chen, Guangduo, Bai, Rui, Huang, Pufeng, Ni, Jie, Chen, Lianglong. 2024. Generation of a homozygous DNAJC19 knockout human embryonic stem cell line by CRISPR/Cas9 system. In Stem cell research, 77, 103427. doi:10.1016/j.scr.2024.103427. https://pubmed.ncbi.nlm.nih.gov/38696852/
2. Janz, Anna, Walz, Katharina, Cirnu, Alexandra, Duff, Henry J, Gerull, Brenda. 2023. Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes. In Molecular metabolism, 79, 101859. doi:10.1016/j.molmet.2023.101859. https://pubmed.ncbi.nlm.nih.gov/38142971/
3. Al Tuwaijri, Abeer, Alyafee, Yusra, Alharbi, Mashael, Umair, Muhammad, Alfadhel, Majid. 2022. Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay. In Molecular genetics & genomic medicine, 10, e1969. doi:10.1002/mgg3.1969. https://pubmed.ncbi.nlm.nih.gov/35611801/
4. Patel, Nisha, Aldahmesh, Mohammed A, Alkuraya, Hisham, Al-Hazzaa, Selwa A F, Alkuraya, Fowzan S. 2015. Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies. In Genetics in medicine : official journal of the American College of Medical Genetics, 18, 554-62. doi:10.1038/gim.2015.127. https://pubmed.ncbi.nlm.nih.gov/26355662/
5. Ojala, Tiina, Polinati, Padmini, Manninen, Tuula, Suomalainen, Anu, Tyni, Tiina. 2012. New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies. In Pediatric research, 72, 432-7. doi:10.1038/pr.2012.92. https://pubmed.ncbi.nlm.nih.gov/22797137/
6. Machiraju, Pranav, Degtiarev, Vlad, Patel, Dhwani, Greenway, Steven C, Khan, Aneal. 2021. Phenotype and pathology of the dilated cardiomyopathy with ataxia syndrome in children. In Journal of inherited metabolic disease, 45, 366-376. doi:10.1002/jimd.12441. https://pubmed.ncbi.nlm.nih.gov/34580891/
7. Davey, K M, Parboosingh, J S, McLeod, D R, Bridge, P J, Bernier, F P. 2005. Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition. In Journal of medical genetics, 43, 385-93. doi:. https://pubmed.ncbi.nlm.nih.gov/16055927/
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