Molecular genetic diagnosis of Charcot-Marie-Tooth disease as well as tomaculous neuropathy;Molekulargenetische Diagnostik der Charcot-Marie-Tooth'schen Erkrankung (CMT) sowie der tomakulosen Neuropathie (HNPP)

Medizinische Genetik

Volumn 9, Issue 3, 1997, Pages 501-504

  Rautenstrauss, B ^a   Liehr, T ^a   Fuchs, C ^a   Ekici, A ^a   Lauffer, H ^a   Nelis, E ^a   Van Broeckhoven, C ^a   Bathke, K D ^a   Grehl, H ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

CMT; deletion; duplication; HMSN; HNPP

Indexed keywords

MYELIN PROTEIN;

CHROMOSOME 17P; GENE DUPLICATION; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MOLECULAR GENETICS; SHORT SURVEY;

EID: 0030870228     PISSN: 09365931     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

References (26)