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Volumn 27, Issue 1, 2008, Pages 1-12

Charcot-Marie-Tooth disorders with an autosomal recessive mode of inheritance

Author keywords

AR CMT; Axonal CMT; Demyelinating CMT; Molecular diagnostics

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOTYPE PHENOTYPE CORRELATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NEUROPATHOLOGY; NEUROPHYSIOLOGY; PRIORITY JOURNAL; REVIEW;

EID: 38549097704     PISSN: 07225091     EISSN: None     Source Type: Journal    
DOI: 10.5414/NPP27001     Document Type: Review
Times cited : (7)

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