Neuropathic scapuloperoneal syndrome (Davidenkow's syndrome) with chromosome 17p11.2 deletion

Muscle and Nerve

Volumn 32, Issue 5, 2005, Pages 668-671

  Verma, Ashok ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Davidenkow's syndrome; HNPP; Neuropathy; PMP 22; Scapuloperoneal syndrome

Indexed keywords

GENE PRODUCT; NERVE PROTEIN; PERIPHERAL NERVE PROTEIN 22; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CASE REPORT; CHROMOSOME 17P; CHROMOSOME DELETION; CHROMOSOME SIZE; DAVIDENKOW DISEASE; DISEASE ASSOCIATION; FATHER; FEMALE; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES; HEREDITARY SPINAL MUSCULAR ATROPHY; HUMAN; NEUROPATHIC SCAPULOPERONEAL SYNDROME; NEUROPATHY; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; RARE DISEASE; SCHOOL CHILD;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MUSCLE WEAKNESS; SYNDROME;

EID: 27144538630     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.20402     Document Type: Article

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