Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
developmental and epileptic encephalopathy, 32
OMIM:616366
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
09/14/2021
PubMed IDs:
17634333 22612818 25751627 25950944 26648591 27733563 29050392 31054490
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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