Fatma Al-Jasmi

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 2

Top Topics

Staphylococcus Aureus

Gene Expression

Genome Wide Analysis

Peritoneal Dialysis

Top Venues

Orphanet journal of rare diseases

Journal of molecular neuroscience : MN

This page only lists publications with an associated author ORCID identifier.

Publications

Feda E Mohamed, Feda E Mohamed, Eiman Al-Ajmi, Nadia Al Hashmi, Khalid Al-Thihli, Amna Al Futaisi, Watfa Al Mamari, Fathiya Al-Murshedi, Fatma Al-Jasmi
Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families. Orphanet journal of rare diseases 18 (1) (2023)
Feda E Mohamed, Amanat Ali, Amal Al-Tenaiji, Amina Al-Jasmi, Fatma Al-Jasmi
A Type 3 Gaucher-Like Disease Due To Saposin C Deficiency in Two Emirati Families Caused by a Novel Splice Site Variant in the PSAP Gene. Journal of molecular neuroscience : MN 72 (6) (2022)