1. Kong, Yang, Zhao, Lihong, Charette, Jeremy R, Nishina, Patsy M, Naggert, Jürgen K. . An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency. In Human molecular genetics, 27, 3340-3352. doi:10.1093/hmg/ddy238. https://pubmed.ncbi.nlm.nih.gov/29947801/
2. Jurgens, Julie A, Matos Ruiz, Paola M, King, Jessica, Bulyk, Martha L, Engle, Elizabeth C. 2024. Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays. In bioRxiv : the preprint server for biology, , . doi:10.1101/2024.09.12.612713. https://pubmed.ncbi.nlm.nih.gov/39314366/
3. Matkovich, Scot J, Van Booven, Derek J, Cappola, Thomas P, Dorn, Gerald W. . Association of an intronic, but not any exonic, FRMD4B sequence variant and heart failure. In Clinical and translational science, 3, 134-9. doi:10.1111/j.1752-8062.2010.00220.x. https://pubmed.ncbi.nlm.nih.gov/20718813/
4. Houwing-Duistermaat, Jeanine J, Helmer, Quinta, Balliu, Bruna, Tsonaka, Roula, Uh, Hae-Won. 2014. Gene analysis for longitudinal family data using random-effects models. In BMC proceedings, 8, S88. doi:10.1186/1753-6561-8-S1-S88. https://pubmed.ncbi.nlm.nih.gov/25519415/
5. Cappola, Thomas P, Li, Mingyao, He, Jing, Cresci, Sharon, Dorn, Gerald W. 2010. Common variants in HSPB7 and FRMD4B associated with advanced heart failure. In Circulation. Cardiovascular genetics, 3, 147-54. doi:10.1161/CIRCGENETICS.109.898395. https://pubmed.ncbi.nlm.nih.gov/20124441/
6. Humphries, Crystal E, Kohli, Martin A, Nathanson, Lubov, Pericak-Vance, Margaret A, Gilbert, John. . Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease. In Journal of Alzheimer's disease : JAD, 44, 977-87. doi:10.3233/JAD-141989. https://pubmed.ncbi.nlm.nih.gov/25380588/
智鼠故事 
