Deafness, Autosomal Dominant, Due To Mutation In Myo1a MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Deafness, Autosomal Dominant, Due To Mutation In Myo1a
Unique ID: C567266
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567266
Heading Mapped to: Hearing Loss / congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Deafness, Autosomal Dominant, Due To Mutation In Myo1a Preferred

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