Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French population

Neurogenetics

Volumn 1, Issue 2, 1997, Pages 117-123

  Latour, P ^a   Levy N ^b,c   Paret, M ^a   Chapon, F ^d,l   Chazot, G ^e,l   Clavelou, P ^f,l   Couratier, P ^g,l   Dumas, R ^h,l   Ollagnon, E ^i,l   Pouget, J ^b,l   Setiey, A ^j,l   Vallat, J M ^g,l   Boucherat, M ^a   Fontes, M ^c   Vandenberghe, A ^a,k  

^a Hopital de l'Antiquaille   (France)

^b TIMONE HOSPITAL   (France)

^c INSERM   (France)

^d CAEN UNIVERSITY HOSPITAL   (France)

^e HÔPITAL NEUROLOGIQUE   (France)

^f UNIVERSITY HOSPITAL OF CLERMONT FERRAND   (France)

^g LIMOGES UNIVERSITY HOSPITAL   (France)

^h HÔPITAL DU BOCAGE   (France)

ⁱ HÔTEL DIEU   (France)

^j Hôpital de Villefranche   (France)

^k UNIVERSITÉ LYON 1   (France)

^l French CMT Consortium   (France)

more..

Author keywords

Charcot Marie Tooth disease; CMTX; Connexin32 mutations; Frequency; SSCP

Indexed keywords

CONNEXIN 32; DNA; GAP JUNCTION PROTEIN;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CHEMISTRY; CHILD; DEMYELINATING DISEASE; FAMILY HEALTH; FEMALE; FRANCE; GENE DELETION; GENETIC LINKAGE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MEDIAN NERVE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PEDIGREE; POINT MUTATION; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CONNEXINS; DEMYELINATING DISEASES; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; FRANCE; HUMANS; LINKAGE (GENETICS); MALE; MEDIAN NERVE; MIDDLE AGED; MUTATION; PEDIGREE; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE DELETION; X CHROMOSOME;

EID: 0031215473     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100480050017     Document Type: Article

References (30)

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