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Defective SLC17A8 Causes Autosomal Dominant Deafness 25 (DFNA25) - Ontify
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Defective SLC17A8 Causes Autosomal Dominant Deafness 25 (DFNA25)
Instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619076).
Statements about
Defective SLC17A8 Causes Autosomal Dominant Deafness 25 (DFNA25)
Instance Of
Biological Pathway
Part Of
SLC Transporter Disorders
Has Part(s)
Defective SLC17A8 Does Not Exchange Cytosolic L-Glu for Synaptic Vesicle H+
Exact Match
https://identifiers.org/reactome:R-H ...
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