A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case
about
Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the NervesAtomic force microscopy and lamins: A review study towards future, combined investigations.Emergencies in motoneuron disease.Are parents of children with Cockayne syndrome manifesting features of the disorder?: Case reports.Prioritization of Variants Detected by Next Generation Sequencing According to the Mutation Tolerance and Mutational Architecture of the Corresponding Genes.
P2860
A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case
description
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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name
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@ast
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@en
type
label
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@ast
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@en
prefLabel
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@ast
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@en
P2093
P2860
P1433
P1476
A novel lamin A/C gene mutatio ...... nvolvement: report of one case
@en
P2093
Jun Kawamata
Naotoshi Iwahara
Shin Hisahara
Shun Shimohama
Takashi Hayashi
P2860
P2888
P356
10.1186/S12883-015-0269-5
P577
2015-02-20T00:00:00Z
P5875
P6179
1049318582