Publication | Closed Access
Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment
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Citations
16
References
2015
Year
Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyDfnb84 FamilyMolecular GeneticsDisease Gene IdentificationCochlear DevelopmentMedicineVariant InterpretationHearing Loss
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