Is CMTX an axonopathy? [8] (multiple letters)

Neurology

Volumn 52, Issue 2, 1999, Pages 432-433

  Scherer, S S ^a   Fischbeck, K H ^a   Birouk, N ^a   LeGuern, E ^a   Bouche, P ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 32;

CLINICAL ARTICLE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LETTER; MOTOR NERVE CONDUCTION; NERVE BIOPSY; NERVE FIBER; POINT MUTATION; PRIORITY JOURNAL; SURAL NERVE; X CHROMOSOME LINKED DISORDER; GENETIC LINKAGE; GENETICS; NOTE; PATHOLOGY; X CHROMOSOME;

AXONS; CHARCOT-MARIE-TOOTH DISEASE; HUMANS; LINKAGE (GENETICS); X CHROMOSOME;

EID: 0033554936     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.2.432-a     Document Type: Letter

References (10)