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Latest

A novel stop-gain mutation in MSH2 gene among a Persian family fulfilling classic Amsterdam criteria for Lynch Syndrome

Pericytes contribute to the islet basement membranes to promote beta-cell gene expression

Inactivation of GaIU leads to a cell wall-associated polysaccharide defect that reduces the susceptibility of Enterococcus faecalis to bacteriolytic agents

Novel mutations in AIFM1 gene associated with X-linked deafness in a Moroccan family

Radixin modulates the function of outer hair cell stereocilia

Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant Patients

Deletion of Exon 1 in AMER1 in Osteopathia Striata with Cranial Sclerosis

Genetics cause of heterogeneous inherited myopathies in a cohort of Greek patients

A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy.

A Specialized Niche in the Pancreatic Microenvironment Promotes Endocrine Differentiation

Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B

Genetic spectrum of retinal dystrophies in Tunisia

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