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Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis

Functional GenomicsSequencingMendelian DisorderGenetic DisorderMedicineGeneticsChinese FamiliesPathologyMolecular GeneticsDisease Gene IdentificationGenomicsMolecular DiagnosticsBioinformaticsVariant InterpretationHereditary Spherocytosis