Genetic variation in KIFAP3 is associated with an upper motor neuron-predominant phenotype in amyotrophic lateral sclerosis.

Neuro-degenerative diseases

Volumn 8, Issue 6, 2011, Pages 491-495

  Orsetti, V ^a   Pegoraro, E ^b   Cima, V ^b   D'Ascenzo, C ^b   Palmieri, A ^b   Querin, G ^b   Volpe, M ^b   Ermani, M ^b   Angelini, C ^b   Soraru G ^b  

^a UNIVERSITY OF PADOVA   (Italy)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSKELETON PROTEIN; DNA; KIFAP3 PROTEIN, HUMAN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; FEMALE; GENE EXPRESSION; GENETIC VARIABILITY; GENETICS; GENOTYPE; HUMAN; KAPLAN MEIER METHOD; MALE; MIDDLE AGED; MOTONEURON; PATHOLOGY; PHENOTYPE; PHYSIOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; SURVIVAL;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADULT; AGED; AGED, 80 AND OVER; AMYOTROPHIC LATERAL SCLEROSIS; CYTOSKELETAL PROTEINS; DNA; FEMALE; GENE EXPRESSION; GENETIC VARIATION; GENOTYPE; HUMANS; KAPLAN-MEIER ESTIMATE; MALE; MIDDLE AGED; MOTOR NEURONS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SURVIVAL ANALYSIS; YOUNG ADULT;

EID: 85027948689     PISSN: None     EISSN: 16602862     Source Type: Journal    
DOI: 10.1159/000327755     Document Type: Article

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