Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
retinitis pigmentosa 12
OMIM:600105
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
11/16/2022
PubMed IDs:
10508521 11389483 12843338 18055816 19140180 20956273 22065545 23379534 28819299
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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