A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy
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A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy
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2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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2015年论文
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2015年论文
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name
A rare variant (c.863G>T) in e ...... le for spinal muscular atrophy
@en
type
label
A rare variant (c.863G>T) in e ...... le for spinal muscular atrophy
@en
prefLabel
A rare variant (c.863G>T) in e ...... le for spinal muscular atrophy
@en
P2093
P2860
P356
P1476
A rare variant (c.863G>T) in e ...... le for spinal muscular atrophy
@en
P2093
Jin-Li Bai
Wen-Hui Zhang
Yan-Yan Cao
Yu-Wei Jin
P2860
P2888
P304
P356
10.1038/EJHG.2015.213
P577
2015-09-30T00:00:00Z