Submission Details

Submitter:

Classification:
Supportive
GENCC:100009
Gene:
Disease:
KBG syndrome
Orphanet:2332
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
09/14/2021
PubMed IDs:
21782149 23184435
Assertion Criteria:
Submitter Submitted Date:
09/14/2021

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