Muscular dystrophy, becker type
OMIM:300376Mode of inheritance:X-linked recessive
Disease classification:Diseases of the nervous system
Mutations
| Gene Symbol | DMD |
|---|---|
| DNA Change | Exons deletion |
| A.A. Change | |
| Exon/Intron | |
| Mutation Type | deletion |
| Reference | Sbiti A, El Kerch F, Sefiani A.Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients. J Biomed Biotechnol. 2002;2(3):158-160. |
Variant not named according to HGVS recommendations