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.

Export

Export

×

MLA

modern-language-association

APA

apa

Chicago

chicago-fullnote-bibliography

Harvard

harvard-cite-them-right

Vancouver

vancouver-author-date

---

RIS BibTex

Export

×

This document cannot be exported because it belongs to another portal.

Full text

lock_openFull text externo

DOI: 10.3390/IJMS21228554 GOOGLE SCHOLAR lock_openOpen access editor

Data source: Scopus