Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13

Neurology

Volumn 46, Issue 5, 1996, Pages 1311-1318

  Timmerman, V ^a   De Jonghe, P ^a   Spoelders, P ^a   Simokovic, S ^a   Lofgren A ^a   Nelis, E ^a   Vance, J ^b   Martin, J J ^c   Van Broeckhoven, C ^a,c  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b DUKE UNIVERSITY MEDICAL CENTER   (United States)

^c UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 1P; CLINICAL ARTICLE; FEMALE; GENE LOCATION; GENE LOCUS; GENETIC LINKAGE; GENETIC POLYMORPHISM; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; HUMAN TISSUE; PEDIGREE; PRIORITY JOURNAL; X CHROMOSOME;

EID: 0029894937     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.46.5.1311     Document Type: Article

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