- Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome
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Kerkeni N, Kharrat M, Maazoul F, Boudabous H, M’rad R, Trabelsi M
- KMID: 2526873
- J Clin Neurol.
- 2022 Mar;18(2):214-222.
- doi: 10.3988/jcn.2022.18.2.214
Background and Purpose Warburg Micro syndrome (WARBM) is a rare autosomal recessive genetic disease characterized by ocular, neurologic, and endocrine anomalies. WARBM is a phenotypically and genetically heterogeneous syndrome caused... -
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