Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
lissencephaly due to LIS1 mutation
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
05/04/2021
PubMed IDs:
32097630 32097629 33096394
Assertion Criteria:
Submitter Submitted Date:
10/27/2022

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