Analysis of the VSX1 gene in sporadic keratoconus patients from China.

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Analysis of the VSX1 gene in sporadic keratoconus patients from China.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

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2017年論文

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2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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Analysis of the VSX1 gene in sporadic keratoconus patients from China.

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Analysis of the VSX1 gene in sporadic keratoconus patients from China.

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Analysis of the VSX1 gene in sporadic keratoconus patients from China.

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P1476

Analysis of the VSX1 gene in sporadic keratoconus patients from China.

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P2093

Hai-Jian Wu

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Li-Bin Zheng

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Tao Guan

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Xue Wang

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Yu-Feng Yao

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P2860

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.

A gene-specific method for predicting hemophilia-causing point mutations.

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.

Keratoconus is associated with increased copy number of mitochondrial DNA.

Genetics of keratoconus: where do we stand?

VSX1 gene analysis in keratoconus

VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.

Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing.

Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.

Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia.

P2888

s12886-017-0567-3

P304

173

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P31

scholarly article

P356

10.1186/S12886-017-0567-3

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P433

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P478

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P577

2017-09-26T00:00:00Z

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P6179

1091924412

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28950846

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5615802

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