Mutations in the myelin protein zero result in a spectrum of Charcot-Marie-Tooth phenotypes

Acta Myologica

Volumn 23, Issue 1, 2004, Pages 6-9

  Kochañski, Andrzej ^a  

^a MOSSAKOWSKI MEDICAL RESEARCH CENTRE   (Poland)

Author keywords

Charcot Marie Tooth disease.; Myelin Protein Zero gene

Indexed keywords

AMINO ACID; MYELIN PROTEIN; PROTEIN KINASE C;

ALLELE; GENE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; IMMUNOHISTOCHEMISTRY; NONHUMAN; PHENOTYPE; REVIEW;

CHARCOT-MARIE-TOOTH DISEASE; HUMANS; MUTATION; MYELIN P0 PROTEIN; PHENOTYPE;

EID: 2642567837     PISSN: 11282460     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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