Seckel syndrome 8 (Q50349582)
Jump to navigation
Jump to search
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 |
|
Statements
1 reference
2 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference