Heisterkamp N, Mulder MP, Langeveld A, ten Hoeve J, Wang Z, Roe BA, et al. (September 1995). "Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region". Genomics. 29 (2): 451–456. doi:10.1006/geno.1995.9982. PMID8666394.
Iacobazzi V, Lauria G, Palmieri F (September 1997). "Organization and sequence of the human gene for the mitochondrial citrate transport protein". DNA Sequence. 7 (3–4): 127–139. doi:10.3109/10425179709034029. PMID9254007.
Palmieri F (April 2013). "The mitochondrial transporter family SLC25: identification, properties and physiopathology". Molecular Aspects of Medicine. 34 (2–3): 465–484. doi:10.1016/j.mam.2012.05.005. PMID23266187.
Palmieri F (February 2004). "The mitochondrial transporter family (SLC25): physiological and pathological implications". Pflügers Archiv: European Journal of Physiology. 447 (5): 689–709. doi:10.1007/s00424-003-1099-7. PMID14598172. S2CID25304722.
Cohen I, Staretz-Chacham O, Wormser O, Perez Y, Saada A, Kadir R, et al. (February 2018). "A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion". American Journal of Medical Genetics. Part A. 176 (2): 330–336. doi:10.1002/ajmg.a.38574. PMID29226520. S2CID6953669.
Heisterkamp N, Mulder MP, Langeveld A, ten Hoeve J, Wang Z, Roe BA, et al. (September 1995). "Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region". Genomics. 29 (2): 451–456. doi:10.1006/geno.1995.9982. PMID8666394.
Iacobazzi V, Lauria G, Palmieri F (September 1997). "Organization and sequence of the human gene for the mitochondrial citrate transport protein". DNA Sequence. 7 (3–4): 127–139. doi:10.3109/10425179709034029. PMID9254007.
Palmieri F (April 2013). "The mitochondrial transporter family SLC25: identification, properties and physiopathology". Molecular Aspects of Medicine. 34 (2–3): 465–484. doi:10.1016/j.mam.2012.05.005. PMID23266187.
Palmieri F (February 2004). "The mitochondrial transporter family (SLC25): physiological and pathological implications". Pflügers Archiv: European Journal of Physiology. 447 (5): 689–709. doi:10.1007/s00424-003-1099-7. PMID14598172. S2CID25304722.
Cohen I, Staretz-Chacham O, Wormser O, Perez Y, Saada A, Kadir R, et al. (February 2018). "A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion". American Journal of Medical Genetics. Part A. 176 (2): 330–336. doi:10.1002/ajmg.a.38574. PMID29226520. S2CID6953669.
Palmieri F (February 2004). "The mitochondrial transporter family (SLC25): physiological and pathological implications". Pflügers Archiv: European Journal of Physiology. 447 (5): 689–709. doi:10.1007/s00424-003-1099-7. PMID14598172. S2CID25304722.
Cohen I, Staretz-Chacham O, Wormser O, Perez Y, Saada A, Kadir R, et al. (February 2018). "A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion". American Journal of Medical Genetics. Part A. 176 (2): 330–336. doi:10.1002/ajmg.a.38574. PMID29226520. S2CID6953669.