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p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome

Developmental AnomalyP.r672c MutationDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsClinical GeneticsPathologyFreeman-sheldon SyndromeMolecular GeneticsDisease Gene IdentificationMedicineEpigeneticsMonogenic DisordersEgyptian Infant