Novel linkage of LMNA Single Nucleotide Polymorphism with Dilated Cardiomyopathy in an Indian case study.

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Novel linkage of LMNA Single Nucleotide Polymorphism with Dilated Cardiomyopathy in an Indian case study.

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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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Novel linkage of LMNA Single N ...... pathy in an Indian case study.

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Novel linkage of LMNA Single N ...... pathy in an Indian case study.

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prefLabel

Novel linkage of LMNA Single N ...... pathy in an Indian case study.

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P1476

Novel linkage of LMNA Single N ...... pathy in an Indian case study.

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P2093

Avinanda Banerjee

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Kaushik Sengupta

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Pradip K Ghoshal

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P2860

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and F

Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.

Polymorphisms in LMNA and near a SERPINA gene cluster are associated with cognitive function in older people.

Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.

P304

99-105

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P31

scholarly article

P356

10.1016/J.IJCHA.2015.02.008

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P478

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P577

2015-02-28T00:00:00Z

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P5875

273834627

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P698

28785654

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P921

single-nucleotide polymorphism

P932

5497236

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