| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8314403 | Clinica Chimica Acta | 2012 | 6 Pages |
Abstract
⺠Two families with SMN1-deleted individuals in two continuous generations were reported. ⺠Genotype-phenotype analysis convinces that SMN2 is an important modifier of SMA. ⺠SMN2 copy number should be considered in the prenatal diagnosis of SMA.
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Authors
Wan-Jin Chen, Jin He, Qi-Jie Zhang, Qi-Fang Lin, Ya-Fang Chen, Xiao-Zhen Lin, Min-Ting Lin, Shen-Xing Murong, Ning Wang,