Identification of a 4 bp deletion (1560del4) in po gene in a family with severe Charcot-Marie-Tooth disease.

Human mutation

Volumn 7, Issue 4, 1996, Pages 377-378

  Bellone, E ^a   Mandich, P ^a   James, R ^a   Nelis, E ^a   Lamba, L D ^a   Van Broeckhoven, C ^a   Ajmar, F ^a  

^a UNIVERSITY OF GENOA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME MAP; ELECTROPHYSIOLOGY; EXON; GENE DELETION; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NERVE CONDUCTION; PATHOPHYSIOLOGY; PERIPHERAL NERVOUS SYSTEM; POLYMERASE CHAIN REACTION;

ADOLESCENT; ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; ELECTROPHYSIOLOGY; EXONS; HUMANS; MYELIN P0 PROTEIN; NEURAL CONDUCTION; PERIPHERAL NERVOUS SYSTEM; POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

EID: 0029693361     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.1380070403     Document Type: Article

References (0)