Spinal Muscular Atrophy and Its Molecular Genetics
Spinal muscular atrophy (SMA) is one of the most common autosomal recessive diseases, affecting aproximately 1 in 6,000 - 10,000 live births, and with a carrier frequency of aproximately 1 in 40- 60. The childhood SMAs can be classified clinically into three groups. Type I (Werdnig-Hoffmann) is the...
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | Turkish |
| Published: |
Cukurova University Faculty of Medicine
2012-02-01
|
| Series: | Arsiv Kaynak Tarama Dergisi |
| Subjects: | |
| Online Access: | http://www.scopemed.org/fulltextpdf.php?mno=20592 |