Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
SELENON-related myopathy
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
07/16/2020
PubMed IDs:
11528383 28558865 32154989 29172004 15961312 25808192 28688748 29850975 15792869 21670436 31066047 26841830 30642275 17951086 23394784 26780752 28606403 15668457 16498447 12192640 20937510
Public Report:
Assertion Criteria:
Submitter Submitted Date:
01/17/2025

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