Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Nature Genetics

Volumn 37, Issue 10, 2005, Pages 1044-1046

  Kuhlenbäumer, Gregor ^a,b   Hannibal, Mark C ^c   Nelis, Eva ^b   Schirmacher, Anja ^a   Verpoorten, Nathalie ^b   Meuleman, Jan ^b,c   Watts, Giles D J ^c   De Vriendt, Els ^b   Young, Peter ^a   Stögbauer, Florian ^a   Halfter, Hartmut ^a   Irobi, Joy ^b   Goossens, Dirk ^b   Del Favero, Jurgen ^b   Betz, Benjamin G ^c   Hor, Hyun ^a   Kurlemann, Gert ^a   Bird, Thomas D ^d,e   Airaksinen, Eila ^f   Mononen, Tarja ^g   Serradell, Adolfo Pou ^h   Prats, José M ⁱ   Van Broeckhoven, Christine ^b   De Jonghe, Peter ^b,j   Timmerman, Vincent ^b   Ringelstein, E Bernd ^a   Chance, Phillip F ^c,d   more..

^a UNIVERSITY OF MÜNSTER   (Germany)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF WASHINGTON   (United States)

^e VA PUGET SOUND HEALTH CARE SYSTEM   (United States)

^f UNIVERSITY OF EASTERN FINLAND   (Finland)

^g KUOPIO UNIVERSITY HOSPITAL   (Finland)

^h UNIVERSITY OF BARCELONA   (Spain)

ⁱ HOSPITAL DE CRUCES   (Spain)

^j ANTWERP UNIVERSITY HOSPITAL   (Belgium)

more..

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; SEPTIN; SEPTIN 9; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRACHIAL PLEXUS; CARCINOGENESIS; CELL DIVISION; CHROMOSOME 17Q; CONTROLLED STUDY; CYTOSKELETON; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY NEURALGIC AMYOTROPHY; HUMAN; MULTIGENE FAMILY; MUSCLE ATROPHY; NEUROPATHY; PRIORITY JOURNAL; PROTEIN FAMILY; PROTEIN FUNCTION;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BRACHIAL PLEXUS NEURITIS; CHROMOSOMES, HUMAN, PAIR 17; DOGS; GTP PHOSPHOHYDROLASES; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MUTATION; RATS;

EID: 27144483990     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1649     Document Type: Article

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