Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosis

Neurobiology of Aging

Volumn 33, Issue 1, 2012, Pages 210.e9-210.e10

  Solski, Jennifer A ^a   Williams, Kelly L ^a,b   Yang, Shu ^a   Nicholson, Garth A ^a,b,c   Blair, Ian P ^a,b  

^a ANZAC RESEARCH INSTITUTE   (Australia)

^b UNIVERSITY OF SYDNEY   (Australia)

^c Department of Microbiology and Infectious Diseases   (Australia)

Author keywords

Amyotrophic lateral sclerosis; Gene; Mutation; Optineurin

Indexed keywords

CYSTEINE; LEUCINE; SERINE; THREONINE;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; COHORT ANALYSIS; CONTROLLED STUDY; GENE; GENE MUTATION; GENETIC CONSERVATION; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; OPTINEURIN GENE; PATHOGENESIS; PEDIGREE ANALYSIS; PREDICTION; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION;

EID: 81355127355     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2011.09.023     Document Type: Article

References (4)

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