Charcot-Marie-Tooth disease type 2 and P0 gene mutations [7] (multiple letters)

Neurology

Volumn 52, Issue 5, 1999, Pages 1110-1111

  Pareyson, D ^a   Sghirlanzoni, A ^a   Bolti, S ^a   Ciano, C ^a   Fallica, E ^a   Mora, M ^a   Taroni, F ^a   Marrosu, M G ^a   Vaccargiu, S ^a   Marrosu, G ^a   Vannelli, A ^a   Cianchetti, C ^a   Muntoni, F ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

DEMYELINATION; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LETTER; MISSENSE MUTATION; MULTIGENE FAMILY; NERVE BIOPSY; NEUROPATHY; PRIORITY JOURNAL;

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

EID: 0033596833     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)