Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
Rett syndrome
OMIM:312750
Mode Of Inheritance:
X-linked dominant
Evaluated Date:
07/22/2015
PubMed IDs:
16630165 10854091 15034579 11214906 11022934 12481990 19034540 10814718 11313756 10767337 15857422 18989701 11930274 10508514 10577905
Assertion Criteria:
Submitter Submitted Date:
11/25/2020

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