Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stages.

International journal of molecular medicine

Volumn 1, Issue 2, 1998, Pages 333-337

  Rautenstrauss, B ^a   Liehr, T ^a   Fuchs, C ^a   Bevot, A ^a   Bornemann, A ^a   Postler, E ^a   Meyermann, R ^a   Uhlhaas, S ^a   Friedl, W ^a   Michaelis, R ^a  

^a UNIVERSITY HOSPITAL ERLANGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 17; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MOSAICISM; ONSET AGE; PRESCHOOL CHILD;

AGE OF ONSET; CHARCOT-MARIE-TOOTH DISEASE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MOSAICISM;

MLCS; MLOWN;

EID: 0031987854     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.1.2.333     Document Type: Article

References (0)