Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

Annals of Neurology

Volumn 42, Issue 6, 1997, Pages 866-872

  Schenone, Angelo ^a   Nobbio, Lucilla ^a   Caponnetto, Claudia ^a   Abbruzzese, Michele ^a   Mandich, Paola ^a   Bellone, Emilia ^a   Ajmar, Franco ^a   Gherardi, Gianfranco ^a   Windebank, Anthony J ^b   Mancardi, Gianluigi ^a  

^a UNIVERSITY OF GENOA   (Italy)

^b MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME 17P; CLINICAL ARTICLE; GENE DELETION; HERITABILITY; HUMAN; NERVE FIBER GROWTH; NEUROPATHY; PARALYSIS; PHENOTYPE; PRIORITY JOURNAL; SURAL NERVE;

CHARCOT-MARIE-TOOTH DISEASE; DOWN-REGULATION; HUMANS; MYELIN PROTEINS; PHENOTYPE; POLYMERASE CHAIN REACTION; RNA, MESSENGER; RNA-DIRECTED DNA POLYMERASE; SEVERITY OF ILLNESS INDEX; SURAL NERVE;

EID: 0031441542     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420607     Document Type: Article

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