Development Of EZ DNA Diagnostic Kit For The Detection Of Homozygous Deletion Of SMN1 Gene In Spinal Muscular Atrophy (SMA) Patients
Spinal Muscular Atrophy (SMA) is the second most frequent fatal autosomal recessive disorder of childhood. The incidence of this disease is approximately 1 in 10000 live births. SMA is characterized by progressive muscle weakness resulting from degeneration and loss of motor neurons in the anteri...
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| 格式: | Thesis |
| 語言: | English |
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2012
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| 在線閱讀: | http://eprints.usm.my/45661/1/Marini%20Marzuki_HJ.pdf |
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