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4. [Neurodevelopmental impact of a mutation in the RHOBTB2 gene]. Beckers M; Stevens R; Debray FG; Leroy P Rev Med Liege; 2024 Jul; 79(7-8):467-470. PubMed ID: 39129541 [TBL] [Abstract][Full Text] [Related]
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9. Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier. Necpál J; Zech M; Valachová A; Sedláček Z; Bendová Š; Hančárová M; Okáľová K; Winkelmann J; Jech R Parkinsonism Relat Disord; 2020 Aug; 77():87-88. PubMed ID: 32653842 [No Abstract] [Full Text] [Related]
10. A distinctive childhood epilepsy syndrome. Sharawat IK; Suthar R; Sankhyan N BMJ Case Rep; 2019 May; 12(5):. PubMed ID: 31061186 [No Abstract] [Full Text] [Related]
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