Heisterkamp N, Mulder MP, Langeveld A, ten Hoeve J, Wang Z, Roe BA, Groffen J (September 1995). "Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region". Genomics. 29 (2): 451–6. 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): 127–39. 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): 465–84. doi:10.1016/j.mam.2012.05.005. PMID23266187.
Palmieri F (February 2004). "The mitochondrial transporter family (SLC25): physiological and pathological implications". Pflügers Archiv. 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, Birk OS (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, Groffen J (September 1995). "Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region". Genomics. 29 (2): 451–6. 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): 127–39. 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): 465–84. doi:10.1016/j.mam.2012.05.005. PMID23266187.
Palmieri F (February 2004). "The mitochondrial transporter family (SLC25): physiological and pathological implications". Pflügers Archiv. 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, Birk OS (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. 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, Birk OS (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.