Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

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The molecular basis of talin2's high affinity toward β1-integrin.Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing.Mechanical unfolding reveals stable 3-helix intermediates in talin and α-catenin.

P2860

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P2860

Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

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2016 nî lūn-bûn

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2016年の論文

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Exome Sequencing of a Pedigree ...... of Fifth Finger Camptodactyly.

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Hao Deng

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Hong Yuan

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Hongbo Xu

http://www.w3.org/2001/XMLSchema#string

Jianguo Zhang

http://www.w3.org/2001/XMLSchema#string

Liping Guan

http://www.w3.org/2001/XMLSchema#string

Shengbo Yang

http://www.w3.org/2001/XMLSchema#string

Xiong Deng

http://www.w3.org/2001/XMLSchema#string

Yi Guo

http://www.w3.org/2001/XMLSchema#string

Yulan Chen

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P2860

Exome sequencing identifies ZNF644 mutations in high myopia

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome

A novel membrane-dependent on/off switch mechanism of talin FERM domain at sites of cell adhesion

A method and server for predicting damaging missense mutations

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

MutationTaster evaluates disease-causing potential of sequence alterations

Talin depletion reveals independence of initial cell spreading from integrin activation and traction.

Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.

Analysis of the mammalian talin2 gene TLN2.

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e0155180

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10.1371/JOURNAL.PONE.0155180

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English

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Han-Xiang Deng

Sheng Deng

Lamei Yuan

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2016-05-25T00:00:00Z

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27223613

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Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

about

P2860

P2860

Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

description

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