ey0018.6-3 | Basic and Genetic Research of DSD | ESPEYB18
E Ilaslan
, R Markosyan
, P Sproll
, BJ Stevenson
, M Sajek
, MP Sajek
, H Hayrapetyan
, T Sarkisian
, L Livshits
, S Nef
, J Jaruzelska
, K Kusz-Zamelczyk
Int J Mol Sci. 2020 Nov 9;21(21):8403. doi: 10.3390/ijms21218403. PMID: 33182400This case report describes a patient with clinically diagnosed partial androgen insensitivity syndrome (PAIS). However, no mutation in the androgen receptor gene was identified. Instead, whole genome sequencing revealed a heterozygous point mutation inherited from the mother in the FKBP4 gene. This gene i...