Progranulin mutations in Dutch familial frontotemporal lobar degeneration

European Journal of Human Genetics

Volumn 15, Issue 3, 2007, Pages 369-374

  Bronner, Iraad F ^a   Rizzu, Patrizia ^a   Seelaar, Harro ^b   van Mil, Saskia E ^a   Anar, Burcu ^a   Azmani, Asma ^b   Kaat, Laura Donker ^b   Rosso, Sonia ^b   Heutink, Peter ^a   van Swieten, John C ^b  

^a VU UNIVERSITY AMSTERDAM   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; PROGRANULIN; UBIQUITIN;

ADULT; ARTICLE; CHROMOSOME 17Q; CONTROLLED STUDY; DEGENERATIVE DISEASE; EXON; FAMILIAL DISEASE; FEMALE; FRAMESHIFT MUTATION; FRONTAL LOBE; GENE FREQUENCY; GENE MUTATION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NETHERLANDS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; POPULATION RESEARCH; PRIORITY JOURNAL; TEMPORAL LOBE;

AGED; AMINO ACID SEQUENCE; ANIMALS; CODON, NONSENSE; DEMENTIA; FEMALE; FRAMESHIFT MUTATION; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NETHERLANDS; PEDIGREE;

EID: 33847183187     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201772     Document Type: Article

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