Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
hypokalemic periodic paralysis, type 1
OMIM:170400
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
10/06/2023
PubMed IDs:
15534250 17330043 18835861 19118277 19225109 21845430 23187123 8605978 9512357
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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