Seckel syndrome 10 (Q50349581)
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Seckel syndrome that has material basis in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24
- SCKL10
- Seckel Syndrome 10
- Seckel Syndrome type 10
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Seckel syndrome 10 |
Seckel syndrome that has material basis in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24 |
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