YearTitlePublication or InstitutionLead Author
2022Aromatase deficiency caused by mutation of CYP19A1 gene:
A case report
J Cent South UnivLI Hongli1, FU Songbo1, DAI Ruchun2, SHENG Zhifeng2, LIUWei2
2022A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase DeficiencyNil Ratan Sircar Medical CollegeDeep Hathi , Soumik Goswami , Nilanjan Sengupta , Arjun Baidya
2020Puberty in patients with aromatase disordersScienceDirect, ElsevierFukami
2020Aromatase Deficiency in a Tall ManSSKM Hospital West Bengal, IndiaPankaj Singhania Debasish Dash
Abhranil Dhar
Pritam Biswas
Piyas Gargari
Rana Bhattacharjee Subhankar Chowdhury Dipanjana Datta Emili Banerjee
2020A novel compound heterozygous variant in CYP19A1
resulting in aromatase deficiency with normal ovarian
tissue
Turkish Journal of PediatricsSezer Acar1 , İbrahim Mert Erbaş1 , Ahu Paketçi1 , Hüseyin Onay2 ,
Tufan Çankaya3 , Semra Gürsoy4 , Bayram Özhan5 , Ayhan Abacı1 ,
Erdener Özer6 , Mustafa Olguner7 , Ece Böber1 , Korcan Demir1
2009Genetic and Clinical Spectrum of
Aromatase Deficiency in Infancy,
Childhood and Adolescence
Hormone ResearchA. Belgorosky
G. Guercio C. Pepe N. Saraco M.A. Rivarola
1993
Molecular basis of aromatase deficiency in an adult female with sexual infantilism and polycystic ovaries
GeneticsYuji Ito
1992Biochemical and molecular genetic analyses on placental aromatase (P-450AROM) deficiency.Journal of Biological ChemistryNobuhiro HaradaSO, Hisamitsu OgawaS, Makio Shozull, Kazuyo YamadaS, Katsuko Suharall