Prion codon 129 homozygosity and sporadic inclusion body myositis [1] [multiple letters]

Neurology

Volumn 57, Issue 2, 2001, Pages 368-

  Lampe, J ^a   Gossrau G ^a,a   Reichmann, H ^a,a   Walter, M C ^a   Mendel, B ^a,a   MS, H ^a   Lochmuller H ^a,a   Orth, M ^a   Schapira, A H V ^a   Koch, R ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN;

CODON; ETHNIC GROUP; GENETIC ANALYSIS; GENETIC PREDISPOSITION; GENOTYPE; GERMANY; HOMOZYGOSITY; HUMAN; INCLUSION BODY MYOSITIS; LETTER; PRIORITY JOURNAL;

EID: 0035943106     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.57.2.368     Document Type: Letter

References (0)