Seckel syndrome 8 (Q50349582)
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Seckel syndrome that has material basis in homozygous mutation in the DNA2 gene on chromosome 10q21
- SCKL8
- SECKEL SYNDROME 8; SCKL8
- Seckel Syndrome type 8
- SECKEL SYNDROME 8
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Seckel syndrome 8 |
Seckel syndrome that has material basis in homozygous mutation in the DNA2 gene on chromosome 10q21 |
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