Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
autosomal dominant nonsyndromic hearing loss 9
Deafness, autosomal dominant 9
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
09/12/2022
PubMed IDs:
10400989 10891988 16078052 20228067 23767834 25049087 251472 25230692 25780252 25788563 26256111 9806553 9931344
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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