Becker muscular dystrophy
SaudiVarKB evidence summary derived from retained literature mentions.
4Phenotype mentions
4Publications
1Associated gene records
0Associated variant records
Associated gene records
Co-mentioned in the same publications| Gene | Identifier / context | Articles | Mentions |
|---|---|---|---|
| LAMA2 | HGNC:6482 | 1 | 1 |
Associated variant records
Co-mentioned in the same publicationsNo retained variant associations.
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Saudi Arabia | — | 1 | 1 |
| Population record | — | 1 | 1 |
| Saudi Arabia · Riyadh | Cohort 41 | 1 | 1 |
Supporting publications
4 records- 2026Total intravenous anesthesia for cardiac transplantation in a teenager with Becker muscular dystrophy: A case report.Saudi journal of anaesthesia1 mentions
- 2010Deletion mutations in Duchenne muscular dystrophy (DMD) in Western Saudi children.Saudi journal of biological sciences1 mentions
- 2002Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.Saudi medical journal1 mentions
- 1997Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain.Human molecular genetics1 mentions