Hereditary demyelinating neuropathy of infancy: A genetically complex syndrome (Multiple letters) [1]

Brain

Volumn 120, Issue 11, 1997, Pages 2113-2115

  Gambardella, A ^a   Muglia, M ^a   Quattrone, A ^a   Tyson, J ^a   Ellis, D ^a   Fairbrother, U ^a   King, R H M ^a   Muntoni, F ^a   Jacobs, J ^a   Malcolm, S ^a   Thomas, P K ^a  

^a Facolta di Medicina   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN;

CHILD; CHROMOSOME 11; DEMYELINATING NEUROPATHY; GENE MAPPING; GENE MUTATION; GENOTYPE; HUMAN; LETTER; MYELIN SHEATH; NONHUMAN; PRIORITY JOURNAL;

CHARCOT-MARIE-TOOTH DISEASE; DEMYELINATING DISEASES; GENETIC DISEASES, INBORN; HUMANS; INFANT; LINKAGE (GENETICS);

EID: 0030859638     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/120.11.2113     Document Type: Letter

References (0)