Posterior amorphous corneal dystrophy caused by a de novo deletion.

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Posterior amorphous corneal dystrophy caused by a de novo deletion.

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh

2016年學術文章

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name

Posterior amorphous corneal dystrophy caused by a de novo deletion.

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Posterior amorphous corneal dystrophy caused by a de novo deletion.

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label

Posterior amorphous corneal dystrophy caused by a de novo deletion.

@en

Posterior amorphous corneal dystrophy caused by a de novo deletion.

@nl

prefLabel

Posterior amorphous corneal dystrophy caused by a de novo deletion.

@en

Posterior amorphous corneal dystrophy caused by a de novo deletion.

@nl

P1476

Posterior amorphous corneal dystrophy caused by a de novo deletion.

@en

P2093

C Cassiman

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I Casteels

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K Devriendt

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M Dieltiëns

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M-T Hua

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S Odent

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P2860

Mutations in KERA, encoding keratocan, cause cornea plana

An anti-proliferative gene BTG1 regulates angiogenesis in vitro

IC3D classification of corneal dystrophies--edition 2

Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene

Axial Growth and Changes in Lenticular and Corneal Power during Emmetropization in Infants

Novel decorin mutation in a Chinese family with congenital stromal corneal dystrophy.

A novel mutation of the decorin gene identified in a Korean family with congenital hereditary stromal dystrophy.

The genetics of cornea plana congenita.

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.

A novel KERA mutation associated with autosomal recessive cornea plana.

P304

167-170

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P31

scholarly article

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10.3109/13816810.2016.1164194

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P577

2016-04-20T00:00:00Z

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P698

27096414

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P921

posterior amorphous corneal dystrophy