Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Section for Clinical Neurogenetics, |
RCV001030783 | SCV001156092 | uncertain significance | Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B | 2019-08-01 | no assertion criteria provided | research |