A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient

Neurobiology of Aging

Volumn 32, Issue 3, 2011, Pages 552.e1-552.e6

  Corrado, Lucia ^a   Carlomagno, Yari ^a   Falasco, Luca ^a   Mellone, Simona ^a   Godi, Michela ^a   Cova, Emanuela ^b   Cereda, Cristina ^b   Testa, Lucia ^a   Mazzini, Letizia ^a   D'Alfonso, Sandra ^a  

^a UNIVERSITY OF EASTERN PIEDMONT   (Italy)

^b C MONDINO NATIONAL NEUROLOGICAL INSTITUTE   (Italy)

Author keywords

Amyotrophic lateral sclerosis; Mutation; Peripherin; PRPH gene; Sporadic

Indexed keywords

PERIPHERIN;

3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION; ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CONTROLLED STUDY; EXON; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC SCREENING; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRON; ITALY; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN STRUCTURE; PRPH GENE;

EID: 79952899321     PISSN: 01974580     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2010.02.011     Document Type: Article

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