1. Golubeva, Volha A, Dorn, Lisa E, Gilbert, Christopher J, Terentyev, Dmitry, Accornero, Federica. 2023. Loss of YTHDF2 Alters the Expression of m6A-Modified Myzap and Causes Adverse Cardiac Remodeling. In JACC. Basic to translational science, 8, 1180-1194. doi:10.1016/j.jacbts.2023.03.012. https://pubmed.ncbi.nlm.nih.gov/37791304/
2. Ochoa, Juan Pablo, Lalaguna, Laura, Mirelis, Jesús G, Lara-Pezzi, Enrique, Garcia-Pavia, Pablo. 2024. Biallelic Loss of Function Variants in Myocardial Zonula Adherens Protein Gene (MYZAP) Cause a Severe Recessive Form of Dilated Cardiomyopathy. In Circulation. Heart failure, 17, e011226. doi:10.1161/CIRCHEARTFAILURE.123.011226. https://pubmed.ncbi.nlm.nih.gov/38436102/
3. Maver, Ales, Zigman, Tamara, Rangrez, Ashraf Yusuf, Baric, Ivo, Peterlin, Borut. 2022. A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathy. In Cold Spring Harbor molecular case studies, 8, . doi:10.1101/mcs.a006221. https://pubmed.ncbi.nlm.nih.gov/35840178/
4. Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Sulem, Patrick, Holm, Hilma, Stefansson, Kari. 2018. Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation. In Communications biology, 1, 68. doi:10.1038/s42003-018-0068-9. https://pubmed.ncbi.nlm.nih.gov/30271950/
5. Jin, M-Q, Huang, B-Y, Lu, D-Y, Huang, J-Y, Ma, L. . Identification and verification of feature biomarkers associated with immune cells in recurrent pregnancy loss. In European review for medical and pharmacological sciences, 28, 556-570. doi:10.26355/eurrev_202401_35053. https://pubmed.ncbi.nlm.nih.gov/38305600/
6. Heliö, Krista, Mäyränpää, Mikko I, Saarinen, Inka, Heliö, Tiina, Koskenvuo, Juha. 2021. GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy. In Frontiers in genetics, 12, 786705. doi:10.3389/fgene.2021.786705. https://pubmed.ncbi.nlm.nih.gov/34899865/
7. Roginski, Raymond S, Lau, Chi W, Santoiemma, Phillip P, Soteropoulos, Patricia, Yang, Jay. 2018. The human GCOM1 complex gene interacts with the NMDA receptor and internexin-alpha. In Gene, 648, 42-53. doi:10.1016/j.gene.2018.01.029. https://pubmed.ncbi.nlm.nih.gov/29339073/
智鼠故事 
