1. Jabbarpour, Neda, Poorshiri, Bita, Saei, Hassan, Barzegar, Mohammad, Bonyadi, Mortaza. . Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion. In Journal of genetics, 102, . doi:. https://pubmed.ncbi.nlm.nih.gov/36823680/
2. Abbasi-Moheb, Lia, Westenberger, Ana, Alotaibi, Maha, Bertoli-Avella, Aida M, Bauer, Peter. 2021. Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathy. In Clinical genetics, 99, 513-518. doi:10.1111/cge.13905. https://pubmed.ncbi.nlm.nih.gov/33354762/
3. Shi, Zhijie, Pang, Yuning, Xu, Xiang, Mai, Kangsen, Ai, Qinghui. 2023. Comparative analysis of nutritional and transcriptional regulation of hacd1 in large yellow croaker (Larimichthys crocea) and rainbow trout (Oncorhynchus mykiss). In Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 266, 110850. doi:10.1016/j.cbpb.2023.110850. https://pubmed.ncbi.nlm.nih.gov/36990141/
4. Konishi, Hiroyuki, Okuda, Ayaka, Ohno, Yusuke, Kihara, Akio. 2010. Characterization of HACD1 K64Q mutant found in arrhythmogenic right ventricular dysplasia patients. In Journal of biochemistry, 148, 617-22. doi:10.1093/jb/mvq092. https://pubmed.ncbi.nlm.nih.gov/20724468/
5. Zhang, Kai, Qian, Ying, Quan, Xiaowei, Zhu, Tengteng, Qian, Biyun. 2022. A Novel Signature of Lipid Metabolism-Related Gene Predicts Prognosis and Response to Immunotherapy in Lung Adenocarcinoma. In Frontiers in cell and developmental biology, 10, 730132. doi:10.3389/fcell.2022.730132. https://pubmed.ncbi.nlm.nih.gov/35295857/
6. Xu, Yingkun, Jin, Yudi, Gao, Shun, Jiang, Linshan, Liu, Shengchun. 2022. Prognostic Signature and Therapeutic Value Based on Membrane Lipid Biosynthesis-Related Genes in Breast Cancer. In Journal of oncology, 2022, 7204415. doi:10.1155/2022/7204415. https://pubmed.ncbi.nlm.nih.gov/36059802/