Variants of STAR, AMH and ZFPM2/FOG2 may contribute towards the broad phenotype observed in 46,XY DSD patients with heterozygous variants of NR5A1

  1. de LaPiscina, I.M.
  2. Mahmoud, R.A.A.
  3. Sauter, K.-S.
  4. Esteva, I.
  5. Alonso, M.
  6. Costa, I.
  7. Rial-Rodriguez, J.M.
  8. Rodríguez-Estévez, A.
  9. Vela, A.
  10. Castano, L.
  11. Flück, C.E.
Aldizkaria:
International Journal of Molecular Sciences

ISSN: 1422-0067,  1661-6596

Argitalpen urtea: 2020

Alea: 21

Zenbakia: 22

Orrialdeak: 1-18

Mota: Artikulua

DOI: 10.3390/IJMS21228554 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus