5 Mayıs 2022

Mutation profile of the patients diagnosed with myeloid

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14 Haziran 2022

Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular diseases

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2 Temmuz 2022

Clinical, Genetic, and Outcome Characteristics of Pediatric Patients

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4 Temmuz 2022

Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia

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