Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
Wolfram-like syndrome
OMIM:614296
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
10/09/2020
PubMed IDs:
11709537 12073007 16648378 18544103 20069065 21538838 25250959 27395765 28802351 29529044 12754709 16151413 21446023 21602428
Public Report:
Assertion Criteria:
Submitter Submitted Date:
11/09/2020

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