Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
severe early-childhood-onset retinal dystrophy
OMIM:248200
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
06/12/2023
PubMed IDs:
21510770 25312043 26780318 28327576 28446513 32278709
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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