Delayed-onset of progressive pseudorheumatoid dysplasia in a Chinese adult with a novel compound WISP3 mutation: a case report.

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Delayed-onset of progressive pseudorheumatoid dysplasia in a Chinese adult with a novel compound WISP3 mutation: a case report.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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name

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@en

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@nl

type

Item

label

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@en

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@nl

prefLabel

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@en

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@nl

P1476

Delayed-onset of progressive p ...... WISP3 mutation: a case report.

@en

P2093

Chengde Yang

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Hui Shi

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Jialin Teng

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Jing Liu

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Jiucun Wang

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Qiongyi Hu

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Xinyao Wu

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Yi Wang

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Yue Sun

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P2860

Functions and mechanisms of action of CCN matricellular proteins

The CCN family of proteins: structure-function relationships

Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia

Progressive pseudorheumatoid dysplasia: report of a family and review.

Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.

Novel WISP3 mutations causing progressive pseudorheumatoid dysplasia in two Chinese families

The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals.

WISP3-dependent regulation of type II collagen and aggrecan production in chondrocytes.

Identification of a mutation in the WISP3 gene in three unrelated families with progressive pseudorheumatoid dysplasia.

A novel compound WISP3 mutation in a Chinese family with progressive pseudorheumatoid dysplasia.

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scholarly article

case report

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10.1186/S12881-017-0507-3

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