Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B [4]

American Journal of Human Genetics

Volumn 59, Issue 1, 1996, Pages 258-262

  Vance, J M ^a   Speer, M C ^a   Stajich, J M ^a   West, S ^a   Wolpert, C ^a   Gaskell, P ^a   Lennon, F ^a   Tim, R M ^a   Rozear, M ^a   Othmane, K B ^a   Pericak Vance, M A ^a   Yee, W C ^a   Elliott, J L ^a   Kwon, J M ^a   Goodfellow, P ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTONOMIC NEUROPATHY; CHROMOSOME 3Q; DIFFERENTIAL DIAGNOSIS; FOOT ULCER; GENE FREQUENCY; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LEG AMPUTATION; LETTER; MAJOR CLINICAL STUDY; MUSCLE WEAKNESS; PRIORITY JOURNAL;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE;

EID: 0029943006     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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