Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients.

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Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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Targeted next generation seque ...... CADASIL diagnostics patients.

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Targeted next generation seque ...... CADASIL diagnostics patients.

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Targeted next generation seque ...... CADASIL diagnostics patients.

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Targeted next generation seque ...... CADASIL diagnostics patients.

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Targeted next generation seque ...... CADASIL diagnostics patients.

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Targeted next generation seque ...... CADASIL diagnostics patients.

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P1476

Targeted next generation seque ...... n CADASIL diagnostics patients

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P2093

Lyn R Griffiths

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Neven Maksemous

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Robert A Smith

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P2860

Predicting deleterious amino acid substitutions

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Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation

dbSNP: the NCBI database of genetic variation

A method and server for predicting damaging missense mutations

A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

Notch3 signaling in vascular smooth muscle cells induces c-FLIP expression via ERK/MAPK activation. Resistance to Fas ligand-induced apoptosis

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s40246-016-0093-z

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scholarly article

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10.1186/S40246-016-0093-Z

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Larisa M. Haupt

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2016-11-24T00:00:00Z

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1051794863

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