Clinical Utility Gene Card For: Wolfram Syndrome

Overview

Journal Eur J Hum Genet

Specialty Genetics

Date 2016 May 26

PMID 27222289

Citations 3

Authors

Mariya Moosajee

Patrick Yu-Wai-Man

Cecile Rouzier

Maria Bitner-Glindzicz

Richard Bowman

Affiliations

Soon will be listed here.

Citing Articles

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings.

Zhang X, Xie Y, Xu K, Chang H, Zhang X, Li Y Invest Ophthalmol Vis Sci. 2022; 63(10):9.

PMID: 36098976 PMC: 9482318. DOI: 10.1167/iovs.63.10.9.

Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1.

Salzano G, Rigoli L, Valenzise M, Chimenz R, Passanisi S, Lombardo F Int J Environ Res Public Health. 2022; 19(1).

PMID: 35010780 PMC: 8744633. DOI: 10.3390/ijerph19010520.

Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches.

Jurkute N, Majander A, Bowman R, Votruba M, Abbs S, Acheson J Eur J Hum Genet. 2018; 27(3):494-502.

PMID: 30143805 PMC: 6460557. DOI: 10.1038/s41431-018-0235-y.

References

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