Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.

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Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.

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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

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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

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2017年论文

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2017年论文

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Mutation analysis of TGFBI and ...... nd granular corneal dystrophy.

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Mutation analysis of TGFBI and ...... nd granular corneal dystrophy.

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Mutation analysis of TGFBI and ...... nd granular corneal dystrophy.

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P1476

Mutation analysis of TGFBI and ...... nd granular corneal dystrophy.

@en

P2093

Dapeng Sun

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Peng Chen

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Xianli Du

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P2860

The IC3D classification of the corneal dystrophies

cDNA from human ocular ciliary epithelium homologous to beta ig-h3 is preferentially expressed as an extracellular protein in the corneal epithelium

Clinical outcomes of phototherapeutic keratectomy in eyes with Thiel-Behnke corneal dystrophy.

A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.

A molecular perspective on corneal dystrophies.

Genetics of anterior and stromal corneal dystrophies.

Next-Generation Sequencing Informatics: Challenges and Strategies for Implementation in a Clinical Environment.

Keratoconus associated with corneal granular dystrophy in a patient of Italian origin.

KRT12 mutations and in vivo confocal microscopy in two Japanese families with Meesmann corneal dystrophy.

Next-generation sequencing in health-care delivery: lessons from the functional analysis of rhodopsin.

P2888

s00417-017-3699-5

P31

scholarly article

P356

10.1007/S00417-017-3699-5

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P577

2017-05-31T00:00:00Z

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P6179

1085735269

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P698

28567551

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