Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies

Annals of Neurology

Volumn 40, Issue 4, 1996, Pages 672-675

  Meijerink, Peter H S ^a   Hoogendijk, Jessica E ^b   Gabreëls Festen, Anneke A W M ^c   Zorn, Ina ^a   Veldman, Henk ^b   Baas, Frank ^a   De Visser, Marianne ^a   Bolhuis, Pieter A ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 1Q; CODON; DEMYELINATING NEUROPATHY; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; NERVE BIOPSY; PRESCHOOL CHILD; PRIORITY JOURNAL; SURAL NERVE;

ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; CODON; FEMALE; HUMANS; INFANT; MICROSCOPY, ELECTRON; MYELIN P0 PROTEIN; MYELIN SHEATH; POINT MUTATION; SURAL NERVE;

EID: 0029959083     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410400418     Document Type: Article

References (19)

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