Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region. [electronic resource]
Producer: 19971016Description: 364-8 p. digitalISSN:- 0364-5134
- Axons -- pathology
- Brain Stem -- pathology
- Chromosomes, Human, Pair 5
- Female
- Gene Deletion
- Hereditary Sensory and Autonomic Neuropathies -- complications
- Humans
- Infant, Newborn
- Male
- Microscopy, Electron
- Muscle, Skeletal -- ultrastructure
- Neurons, Afferent -- pathology
- Phenotype
- Spinal Muscular Atrophies of Childhood -- complications
- Sural Nerve -- ultrastructure
No physical items for this record
Publication Type: Case Reports; Comparative Study; Journal Article
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