1)  LMNA
LMNA
1.
No mutation was detected in the LMNA gene among sporadic Charcot-Marie-Tooth patients;
在散发型腓骨肌萎缩症患者中未检测出LMNA基因突变(英文)
2.
The Effect on Cell Mitosis of LMNA Gene Mutation E82K Associated with Familial Dilated Cardio-myopathy;
扩张型心肌病致病基因LMNA突变E82K对细胞分裂的影响
3.
A novel LMNA gene mutation E82K associated with familial dilated cardiomyopathy;
扩张型心肌病致病基因LMNA新突变E82K的发现及其功能的初步研究
2)  LMNA gene
LMNA基因
1.
The EMD gene for the X-linked EDMD encodes emerin protein and the LMNA gene for the autosomal EDMD encodes lamins A/C.
EMD基因和LMNA基因是引起X-连锁EDMD和常染色体遗传EDMD的致病基因,编码产物分别为emerin蛋白和核纤层蛋白(lamin)A/C。
2.
Results We found 1 mutation which was in the seventh intron of LMNA gene,it is single nucleotide polymorphisms(SNPs) .
目的研究中国黄种汉族人特发性扩张型心肌病(IDCM)患者LMNA基因的突变情况。
补充资料：J基因
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性质： 为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。

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