Dejerine-Sottas syndrome grown to maturity: Overview of genetic and morphologicl heterogeneity and follow-up of 25 patients

Journal of Anatomy

Volumn 200, Issue 4, 2002, Pages 341-356

  Gabreëls Festen, Anneke ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

CMT4B; Congenital hypomyelination; Demyelinating HMSN; Focally folded myelin; HMSN type III

Indexed keywords

ADOLESCENT; ADULT; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DEMYELINATING NEUROPATHY; DISABILITY; DISEASE COURSE; DISEASE SEVERITY; FEMALE; FOLLOW UP; GENE MUTATION; GENETIC HETEROGENEITY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOTOR NERVE CONDUCTION; PHENOTYPE; PRIORITY JOURNAL; REVIEW; WALKING; WHEELCHAIR;

ADOLESCENT; ADULT; BIOPSY; CHILD; CHILD, PRESCHOOL; DISABILITY EVALUATION; DISEASE PROGRESSION; FEMALE; FOLLOW-UP STUDIES; GENES, DOMINANT; GENES, RECESSIVE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MUTATION, MISSENSE; MYELIN PROTEINS; SURAL NERVE;

EID: 0036257516     PISSN: 00218782     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-7580.2002.00043.x     Document Type: Review

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