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Forough Sargolzaeiaval
Molecular Genetic Pathology Fellowship · University of California (San Diego) Medical Center
Credentials: ·
History


- 2025–2026

- 2017–2021
Doctor of Medicine
Research
CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures
Case report · Molecular Genetics & Genomic Medicine · 2018 · First of 11 authors · 27 citations
Kidney International · 2024 · 20 citations
Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients
Molecular Syndromology · 2018 · 6 citations
- GM
2 papers

1 paper
- EA
1 paper

1 paper

1 paper · 1 as a resident

1 paper
- MZ
1 paper · 1 as a resident
- PK
1 paper