A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.

BMC neurology

Volumn 10, Issue , 2010, Pages 99-

  Rodríguez Martínez, Ana B ^a   Garrido, Joseba M ^b   Zarranz, Juan J ^b   Arteagoitia, Jose M ^b   de Pancorbo, Marian M ^b   Atarés, Begoña ^b   Bilbao, Miren J ^b   Ferrer, Isidro ^b   Juste, Ramón A ^b  

^a NEIKER and a Vaccine producing Commercial Company CZVSL   (Spain)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN; PROTEINASE K; VALINE;

AGED; ARTICLE; BRAIN; CASE REPORT; CODON; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; PATHOLOGY; PHENOTYPE; PRION DISEASE; WESTERN BLOTTING;

AGED; BLOTTING, WESTERN; BRAIN; CODON; ENDOPEPTIDASE K; GENOTYPE; HUMANS; MALE; METHIONINE; PHENOTYPE; PRION DISEASES; PRPSC PROTEINS; VALINE;

MLCS; MLOWN;

EID: 79952113179     PISSN: None     EISSN: 14712377     Source Type: Journal    
DOI: 10.1186/1471-2377-10-99     Document Type: Article

References (0)