Dejerine-sottas disease with de novo dominant point mutation of the pmp22 gene

Neurology

Volumn 45, Issue 9, 1995, Pages 1766-1767

  Ionasescu, V V ^a   Ionasescu, R ^a   Searby, Ch ^a   Neahring, R ^a  

^a UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN;

ADULT; AMINO ACID SUBSTITUTION; AREFLEXIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; ELECTROMYOGRAM; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HYPESTHESIA; KYPHOSCOLIOSIS; MUSCLE ATROPHY; MUSCLE WEAKNESS; NERVE CONDUCTION; POINT MUTATION; PRIORITY JOURNAL; PROPRIOCEPTION;

ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; CASE REPORT; FEMALE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMAN; MOLECULAR SEQUENCE DATA; MYELIN PROTEINS; POINT MUTATION; POLYMERASE CHAIN REACTION; SUPPORT, NON-U.S. GOV'T;

EID: 0028788494     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.45.9.1766     Document Type: Article

References (0)