Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
Wolfram syndrome 1
OMIM:222300
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
07/16/2020
PubMed IDs:
21602428 11317648 15277431 15070927 25390390 11295831 16459465 16151413 15503287 14724730 21968327 21067485 19160074 15605410 16442662 12707373 22226368 17568405 15151504 9771706 18806274 21623591 20875904 22781099 21446023 21726277 12107816 21564155 22238590 11161832 18660851 19042979 23373429 21823543 22311385 23103830 10521293
Assertion Criteria:
Submitter Submitted Date:
09/11/2023

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