α‐1 antitrypsin phenotypes in demyelinating disease: An association between demyelinating disease and the allele PiM3

Annals of Neurology

Volumn 18, Issue 4, 1985, Pages 514-516

  McCombe, P A ^a   Clark, P ^a   Frith, J A ^a   Hammond, S R ^a   Stewart, G J ^a   Pollard, J D ^a   McLeod, J G ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 1 ANTITRYPSIN;

CENTRAL NERVOUS SYSTEM; DEMYELINATING NEUROPATHY; DIAGNOSIS; GUILLAIN BARRE SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MULTIPLE SCLEROSIS; NERVOUS SYSTEM; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL;

ALLELES; ALPHA 1-ANTITRYPSIN; DEMYELINATING DISEASES; HETEROZYGOTE; HUMANS; MULTIPLE SCLEROSIS; PHENOTYPE; POLYRADICULONEUROPATHY; RISK;

EID: 0022381485     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410180417     Document Type: Article

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