Novel <i>WFS1</i> Variants in Two Moroccan Families with Wolfram Syndrome-Reference-Cited by-同舟云学术

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Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome

Published:2024-06-01 Issue:6 Volume:28 Page:257-262
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Bouhouche Ahmed¹²^ORCID,Sefiani Sara²,Charoute Hicham³,Houyam Tibar¹²,Bouslam Naima²,El Yousfi Fatima-Zahra¹,Bnouhana Wadi¹⁴,Benomar Ali¹²,Ouadghiri Fatima-Zahra¹,Regragui Wafaa¹²

Affiliation:

1. Research Team in Neurology and Neurogenetics, Center of Genomics of Human Pathologies, Medical School and Pharmacy, University Mohammed V in Rabat, Rabat, Morocco.

2. Department of Neurology and Neurogenetics, Specialties Hospital, CHU Ibn Sina, Rabat, Morocco.

3. Research Unit of Epidemiology, Biostatistics and Bioinformatics, Institut Pasteur du Maroc, Casablanca, Morocco.

4. Department of Neurology and Neuropsychology, Specialties Hospital, CHU Ibn Sina, Rabat, Morocco.

Publisher

Mary Ann Liebert Inc

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2023.0550

Reference16 articles.

1. Monogenic diabetes syndromes: Locus-specific databases for Alström, Wolfram, and Thiamine-responsive megaloblastic anemia

2. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome

3. Syndrome de Wolfram familial

4. Selective cognitive and psychiatric manifestations in Wolfram Syndrome

5. Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome

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