1. Beyens, Aude, Moreno-Artero, Ester, Bodemer, Christine, Hadj-Rabia, Smail, Callewaert, Bert. 2018. ATP6V0A2-related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype. In Experimental dermatology, 28, 1142-1145. doi:10.1111/exd.13723. https://pubmed.ncbi.nlm.nih.gov/29952037/
2. Udono, Miyako, Fujii, Kaoru, Harada, Gakuro, Kuhara, Satoru, Katakura, Yoshinori. 2015. Impaired ATP6V0A2 expression contributes to Golgi dispersion and glycosylation changes in senescent cells. In Scientific reports, 5, 17342. doi:10.1038/srep17342. https://pubmed.ncbi.nlm.nih.gov/26611489/
3. Bahena-Bahena, D, López-Valdez, J, Raymond, K, Ruíz-García, M, Martínez-Duncker, I. 2014. ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA. In Molecular genetics and metabolism reports, 1, 203-212. doi:. https://pubmed.ncbi.nlm.nih.gov/27896089/
4. Karacan, İlker, Diz Küçükkaya, Reyhan, Karakuş, Fatma Nur, Hançer, Veysel Sabri, Turanlı, Eda Tahir. 2018. A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing. In Turkish journal of haematology : official journal of Turkish Society of Haematology, 36, 29-36. doi:10.4274/tjh.galenos.2018.2018.0325. https://pubmed.ncbi.nlm.nih.gov/30474613/