Expression of peripheral myelin protein zero in sural nerve of patients with Charcot-Marie-Tooth disease 1B

Pediatric Neurology

Volumn 24, Issue 1, 2001, Pages 33-35

  Tachi, Nobutada ^a   Kozuka, Naoki ^a   Ohya, Kazuhiro ^b   Chiba, Shunzo ^b   Sasaki, Kimio ^c   Uyemura, Keiichi ^d  

^a SAPPORO MEDICAL UNIVERSITY   (Japan)

^b SAPPORO MEDICAL UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c Hokaido Prefectural Rehabilitation Center for Physically Handicapped Children   (Japan)

^d KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; ARGININE; GUANINE; LYSINE; MYELIN PROTEIN; NUCLEOTIDE;

AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; EXON; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOTE; HUMAN; HUMAN TISSUE; IMMUNOBLOTTING; IMMUNOHISTOCHEMISTRY; MOLECULAR WEIGHT; MYELINATED NERVE; NERVE BIOPSY; NUCLEIC ACID BASE SUBSTITUTION; PEDIGREE ANALYSIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCHOOL CHILD; SURAL NERVE;

AMINO ACID SUBSTITUTION; BIOPSY; CHARCOT-MARIE-TOOTH DISEASE; CHILD; EXONS; FEMALE; GENE EXPRESSION; HETEROZYGOTE DETECTION; HUMANS; MUTATION, MISSENSE; MYELIN P0 PROTEIN; NERVE FIBERS, MYELINATED; PEDIGREE; SURAL NERVE;

EID: 0035134428     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(00)00225-3     Document Type: Article

References (18)

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10. Clinical phenotypes of different MPZ (PO) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
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