Molecular Diagnosis and Molecular Mechanism of Spinal Muscular Atrophy
博士 === 高雄醫學大學 === 醫學研究所 === 97 === Spinal muscular atrophy (SMA) is an autosomal recessive disease with high carrier rate, caused by deletion or mutation of survival motor neuron1 (SMN1) gene. There is another gene with almost the same sequence with SMN1 named SMN2, and the deletion or mutation of S...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2009
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| Online Access: | http://ndltd.ncl.edu.tw/handle/90284855578907589944 |