Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.

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cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data The genetics of primary progressive aphasia

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Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.

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2013 nî lūn-bûn

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Exome sequencing reveals a nov ...... g primary progressive aphasia.

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Elizabeth Gordon

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John C Janssen

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Jonathan Beck

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Jonathan M Schott

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Simon Mead

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Tamas Revesz

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Tammaryn Lashley

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P2860

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A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

The heritability and genetics of frontotemporal lobar degeneration.

Phenotypic signatures of genetic frontotemporal dementia.

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scholarly article

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10.1136/JNNP-2013-306116

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English

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2013-07-31T00:00:00Z

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Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.

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P2860

P2860

Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.

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P1476

P2093

P2860

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P356

P407

P433

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P577

P5875

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P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932