Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
hypotonia, ataxia, and delayed development syndrome
OMIM:617330
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
04/26/2023
PubMed IDs:
28017370 28017373
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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