Iughetti, L., Lucaccioni, L., Bruzzi, P., Ciancia, S., Bigi, E., Madeo, S. F., . . . Roucher-Boulez, F. (2019). Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: A case report. BMC Med Genet.
Chicago Style CitationIughetti, Lorenzo, Laura Lucaccioni, Patrizia Bruzzi, Silvia Ciancia, Elena Bigi, Simona Filomena Madeo, Barbara Predieri, i Florence Roucher-Boulez. "Isolated Hypoaldosteronism As First Sign of X-linked Adrenal Hypoplasia Congenita Caused By a Novel Mutation in NR0B1/DAX-1 Gene: A Case Report." BMC Med Genet 2019.
Cita MLAIughetti, Lorenzo, et al. "Isolated Hypoaldosteronism As First Sign of X-linked Adrenal Hypoplasia Congenita Caused By a Novel Mutation in NR0B1/DAX-1 Gene: A Case Report." BMC Med Genet 2019.