Linda Schnapp
0000-0001-8291-1702
Pieris Pharmaceuticals GmbH
3 papers found
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Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
Novel Loss-of-Function Variants in CDC14A are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients
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