Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration. - Test2 - elhamkhani - TriplyDB

Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.

Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.

http://www.wikidata.org/entity/Q37235164

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GRN and MAPT Mutations in 2 Frontotemporal Dementia Research Centers in Brazil.The Role of PGRN in Alzheimer's Disease.

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Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.

http://www.wikidata.org/entity/Q37235164

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 06 March 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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European Journal of Human Genetics

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Novel progranulin mutations wi ...... totemporal lobar degeneration.

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Charlotte Forsell

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Huei-Hsin Chiang

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Håkan Thonberg

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Inger Nennesmo

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Krishnan Shanmugarajan

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Lena Lilius

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Linn Öijerstedt

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Marie Westerlund

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Steinunn Thordardottir

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A harmonized classification system for FTLD-TDP pathology

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

Apolipoprotein E epsilon4 allele has no effect on age at onset or duration of disease in cases of frontotemporal dementia with pick- or microvacuolar-type histology.

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1260-1265

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scholarly article

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10.1038/EJHG.2013.37

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