1. Gupta, Meghana, Kamynina, Elena, Morley, Samantha, Sharma, Gaurav, Manor, Danny. 2013. Plekhg4 is a novel Dbl family guanine nucleotide exchange factor protein for rho family GTPases. In The Journal of biological chemistry, 288, 14522-14530. doi:10.1074/jbc.M112.430371. https://pubmed.ncbi.nlm.nih.gov/23572525/
2. Wieczorek, Stefan, Arning, Larissa, Alheite, Ingrid, Epplen, Jörg T. 2006. Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population. In Journal of human genetics, 51, 363-367. doi:10.1007/s10038-006-0372-y. https://pubmed.ncbi.nlm.nih.gov/16491300/
3. Cagnoli, Claudia, Brussino, Alessandro, Di Gregorio, Eleonora, Durr, Alexandra, Brice, Alexis. . The (-16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients. In Movement disorders : official journal of the Movement Disorder Society, 22, 752-3. doi:. https://pubmed.ncbi.nlm.nih.gov/17290458/
4. Sakai, Haruya, Yoshida, Kunihiro, Shimizu, Yusaku, Ikeda, Shu-ichi, Matsumoto, Naomichi. 2010. Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan. In Neurogenetics, 11, 409-15. doi:10.1007/s10048-010-0245-6. https://pubmed.ncbi.nlm.nih.gov/20424877/
5. Kim, Sungryong, Kim, Namphil, Kang, Hyo-Min, Lee, Amos Chungwon, Na, Ki-Jeong. 2023. Canine Somatic Mutations from Whole-Exome Sequencing of B-Cell Lymphomas in Six Canine Breeds-A Preliminary Study. In Animals : an open access journal from MDPI, 13, . doi:10.3390/ani13182846. https://pubmed.ncbi.nlm.nih.gov/37760246/
6. Carelli, Valerio, Schimpf, Simone, Fuhrmann, Nico, Liguori, Rocco, Wissinger, Bernd. 2011. A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. In Human molecular genetics, 20, 1893-905. doi:10.1093/hmg/ddr071. https://pubmed.ncbi.nlm.nih.gov/21349918/