Rare variants in known and novel candidate genes predisposing to statin-associated myopathy.

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Rare variants in known and novel candidate genes predisposing to statin-associated myopathy.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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Rare variants in known and nov ...... to statin-associated myopathy.

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Rare variants in known and nov ...... to statin-associated myopathy.

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Rare variants in known and nov ...... to statin-associated myopathy.

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P1476

Rare variants in known and nov ...... to statin-associated myopathy

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Jaroslav A Hubáček

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Lenka Mrázová

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Stanislav Kmoch

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Věra Adámková

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P2860

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SLCO1B1 variants and statin-induced myopathy--a genomewide study

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.

GEMINI: integrative exploration of genetic variation and genome annotations.

Integrative data mining highlights candidate genes for monogenic myopathies.

P304

1405-1414

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P31

scholarly article

P356

10.2217/PGS-2016-0071

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P433

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P478

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P577

2016-06-14T00:00:00Z

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P698

27296017

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