Diagnosis of gene dosage alterations at the PMP22 gene using MAPH.

Journal of medical genetics

Volumn 40, Issue 11, 2003, Pages

  Akrami, S M ^a   Rowland, J S ^a   Taylor, G R ^a   Armour, J A ^a  

^a UNIVERSITY OF NOTTINGHAM   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSTIC AGENT; MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

ARTICLE; DNA PROBE; GENE DOSAGE; GENETICS; HEMODYNAMICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; METHODOLOGY; MUTATION; NEUROPATHY; NUCLEIC ACID HYBRIDIZATION; PARALYSIS;

CHARCOT-MARIE-TOOTH DISEASE; DNA PROBES; GENE DOSAGE; HEMODYNAMIC PROCESSES; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; MUTATION; MYELIN PROTEINS; NUCLEIC ACID HYBRIDIZATION; PARALYSIS;

MLCS; MLOWN;

EID: 1542543324     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.11.e123     Document Type: Article

References (0)