28 March 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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13 October 2025

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

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14 October 2025

Genetic characterization and clinicalcorrelation in a cohort of Turkish patientswith immunodeficiency: insights from wholeexome sequencing

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15 October 2025

A novel heterozygous mutation in the SYK gene and systemic inflammation with immunodeficiency – a case report

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