A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family.

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A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family.

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2017年の論文

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2017年学术文章

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A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

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A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

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A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

@en

A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

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A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

@en

A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

@nl

P1476

A Novel KRIT1/CCM1 Gene Insert ...... ormations in a Chinese Family.

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P2093

Hui Wang

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Wei Li

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Xingang Li

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Yongjun Wang

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Yue Suo

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Yunzhu Pan

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Zaiqiang Zhang

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Zhe Xu

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P2860

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)

A perfect message: RNA surveillance and nonsense-mediated decay

Genetics of cavernous angiomas.

Mechanisms of mRNA surveillance in eukaryotes.

Cerebral cavernous malformations. Incidence and familial occurrence.

A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations

Histopathological Features of Brain Arteriovenous Malformations in Japanese Patients.

High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors.

Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.

Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasis.

P2888

s12031-017-0881-5

P304

221-226

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scholarly article

P356

10.1007/S12031-017-0881-5

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P433

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P478

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P577

2017-02-03T00:00:00Z

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P698

28160210

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