Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype
- Resource Type
- Article
- Authors
- Parween, Shaheena; Fernández-Cancio, Mónica; Benito-Sanz, Sara; Camats, Núria; Rojas Velazquez, Maria Natalia; López-Siguero, Juan-Pedro; Udhane, Sameer S; Kagawa, Norio; Flück, Christa E; Audí, Laura; Pandey, Amit V
- Source
- The Journal of Clinical Endocrinology & Metabolism; April 2020, Vol. 105 Issue: 4 pe1272-e1290, 19p
- Subject
- Language
- ISSN
- 0021972X; 19457197