Genetic heterogeneity in hereditary sensory and autonomic neuropathies: The need for improved ascertainment

Muscle and Nerve

Volumn 23, Issue 10, 2000, Pages 1453-1455

  Dyck, Peter J ^a   Dyck, P James B ^a   Schaid, Daniel J ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIFFERENTIAL DIAGNOSIS; EDITORIAL; GENETIC HETEROGENEITY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUSCLE ATROPHY; PRIORITY JOURNAL;

GENETIC HETEROGENEITY; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMAN;

EID: 0033808791     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-4598(200010)23:10<1453::AID-MUS1>3.0.CO;2-4     Document Type: Editorial

References (16)

1. Linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1
2. DNA deletion associated with hereditary neuropathy with liability to pressure palsies
3. Clinical, electrophysiological and genetic study of a family with autosomal dominant hereditary sensory neuropathy and prominent weakness
4. Neuronal atrophy and degeneration predominantly affecting peripheral sensory and autonomic neurons
5. A Virginia kinship with hereditary sensory neuropathy: Peroneal muscular atrophy and pes cavus
6. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy: I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies
7. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy: II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations
8. 'Burning feet' as the only manifestation of dominantly inherited sensory neuropathy
9. Neuronal atrophy and degeneration predominantly affecting peripheral sensory neurons
10. Neurogenic arthropathy and recurring fractures with subclinical inherited neuropathy
11. Severe sensory changes, and trophic disorder, in peroneal muscular atrophy (Charcot-Marie-Tooth type)
12. Hereditary perforating ulcer of the foot
13. DNA duplication associated with Charcot-Marie-Tooth disease type 1A
14. Hereditary sensory neuropathy, type II. Clinical, electrophysiologic, histologic, and biochemical studies of a Quebec kinship
15. Estimating the power of a proposed linkage study for a complex genetic trait
16. Hereditary sensory neuropathy with sensorineural deafness and early-onset dementia