Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome.
Nesrine KerkeniMaher KharratFaouzi MaazoulHela BoudabousRidha M'radMediha TrabelsiPublished in: Journal of clinical neurology (Seoul, Korea) (2022)
(NM_012233.3: c.297del, p.Gln99fs) that is most likely pathogenic and allowed us to confirm the diagnosis of WARBM.
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