Striking PrP sc heterogeneity in inherited prion diseases with the D178N mutation (multiple letters)

Annals of Neurology

Volumn 56, Issue 6, 2004, Pages 909-911

  Haïk, Stéphane ^a,b   Peoc'h, Katell ^c   Brandel, Jean Philippe ^b   Privat, Nicolas ^a   Laplanche, Jean Louis ^c   Faucheux, Baptiste A ^a   Hauw, Jean Jacques ^a   Head, Mark W ^d   Ironside, James W ^d  

^a Inst Natl S/Rech Med U360   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c HÔPITAL LARIBOISIÈRE   (France)

^d UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ISOPROTEIN; METHIONINE; PRION PROTEIN; PROTEASE RESISTANT PRION PROTEIN; UNCLASSIFIED DRUG; VALINE; ASPARAGINE; ASPARTIC ACID;

AMINO ACID SUBSTITUTION; BRAIN REGION; CASE REPORT; CODON; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; FATAL FAMILIAL INSOMNIA; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; HUMAN TISSUE; LETTER; NEUROPATHOLOGY; PRION DISEASE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN TRANSPORT; WESTERN BLOTTING; BRAIN; GENETICS; MUTATION; NOTE; PATHOLOGY;

ASPARAGINE; ASPARTIC ACID; BRAIN; HUMANS; MUTATION; PRION DISEASES; PRPSC PROTEINS;

EID: 9644299705     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20327     Document Type: Letter

References (0)