Rare myelin protein zero sequence variant in late onset CMT1B

Journal of the Neurological Sciences

Volumn 263, Issue 1-2, 2007, Pages 177-179

  Souayah, Nizar ^a   Seltzer, W K ^b   Brannagan, Thomas H ^c   Chin, Russell L ^c   Sander, Howard W ^c,d,e  

^a RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

^b ATHENA DIAGNOSTICS INC   (United States)

^c WEILL CORNELL MEDICAL COLLEGE   (United States)

^d ST VINCENT S HOSPITAL MANHATTAN   (United States)

^e NEW YORK MEDICAL COLLEGE   (United States)

Author keywords

Axonal; Charcot Marie Tooth; Hereditary; Mutation; Myelin protein 0; Neuropathy

Indexed keywords

MYELIN PROTEIN; MYELIN PROTEIN ZERO; UNCLASSIFIED DRUG;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CLINICAL FEATURE; ELECTROMYOGRAPHY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LIMB WEAKNESS; MEDICAL EXAMINATION; MUTATIONAL ANALYSIS; NERVE CONDUCTION; NEUROLOGIC EXAMINATION; ONSET AGE; PRIORITY JOURNAL;

AGED; CHARCOT-MARIE-TOOTH DISEASE; FAMILY HEALTH; FEMALE; HISTIDINE; HUMANS; MIDDLE AGED; MUTATION; MYELIN P0 PROTEIN; NEURAL CONDUCTION; PROLINE;

EID: 35648943770     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jns.2007.05.020     Document Type: Article

References (7)

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