Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood

Journal of Child Neurology

Volumn 11, Issue 2, 1996, Pages 133-146

  Ouvrier, Robert ^a,b  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b UNIVERSITY OF SYDNEY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GAP JUNCTION PROTEIN; MYELIN PROTEIN;

AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 1; CHROMOSOME 17; CHROMOSOME 8; CONFERENCE PAPER; GENE DELETION; GENE DUPLICATION; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HISTOPATHOLOGY; HUMAN; MOLECULAR GENETICS; MYELIN DEFICIENCY; NERVE CONDUCTION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME; X CHROMOSOME DOMINANT DISORDER;

EID: 0029873432     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307389601100214     Document Type: Conference Paper

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