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Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: a Case Report
Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: a Case Report
2019
Moath Hamed
Aakash Shetty
Tara Dzwiniel
Mark Buller
Lotta Koskinen
Oksana Suchowersky
Keywords:
Episodic ataxia
Endocrinology
Compound heterozygosity
Internal medicine
Medicine
Joubert syndrome
Correction
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