Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
03/27/2020
PubMed IDs:
11431692 15258213 16301523 16639411 16804265 17272269 17620490 18971204 20880070 22952820 24076137 24091712 9153451
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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