1. Kavoosian, Saeid, Asgharian, Alimohammad, Asouri, Mohsen, Ebrahimi, Nima, Ataee, Ramin. . Polymorphism of LRP4 Gene (rs9667108) among Post Menopause Women with Osteoporosis. In Iranian journal of public health, 52, 840-847. doi:10.18502/ijph.v52i4.12457. https://pubmed.ncbi.nlm.nih.gov/37551184/
2. Ohno, Kinji, Ohkawara, Bisei, Shen, Xin-Ming, Selcen, Duygu, Engel, Andrew G. 2023. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. In International journal of molecular sciences, 24, . doi:10.3390/ijms24043730. https://pubmed.ncbi.nlm.nih.gov/36835142/
3. Cao, Rangjuan, Chen, Peng, Wang, Hongsheng, Xiong, Wen-Cheng, Mei, Lin. 2023. Intrafusal-fiber LRP4 for muscle spindle formation and maintenance in adult and aged animals. In Nature communications, 14, 744. doi:10.1038/s41467-023-36454-8. https://pubmed.ncbi.nlm.nih.gov/36765071/
4. Chatzinakos, Chris, Pernia, Cameron D, Morrison, Filomene G, Ressler, Kerry J, Daskalakis, Nikolaos P. 2023. Single-Nucleus Transcriptome Profiling of Dorsolateral Prefrontal Cortex: Mechanistic Roles for Neuronal Gene Expression, Including the 17q21.31 Locus, in PTSD Stress Response. In The American journal of psychiatry, 180, 739-754. doi:10.1176/appi.ajp.20220478. https://pubmed.ncbi.nlm.nih.gov/37491937/
5. Khan, Hammal, Ullah, Kifayat, Jan, Abid, Ullah, Imran, Ahmad, Wasim. 2023. A variant in the LDL receptor-related protein encoding gene LRP4 underlying polydactyly and phalangeal synostosis in a family of Pakistani origin. In Congenital anomalies, 63, 190-194. doi:10.1111/cga.12536. https://pubmed.ncbi.nlm.nih.gov/37563890/
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