Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
OMIM:125310
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
08/23/2023
PubMed IDs:
11486103 11571335 12482954 15210536 15364702 16864835 19153638 22623959 23151434 23572112 24000151 24277202 24425116 24844136 25260852 25394726 25870235 28710804 30855338 32122318 35302383
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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