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Homo sapiens chromosome 17, clone RP11-978P20, complete sequence
Homo sapiens chromosome 17, clone RP11-978P20, complete sequence
gi|168823631|gnl|WIBR|L35457|gb|AC2 .1|
Nucleotide
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Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Autonomic Neuropathies
A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There ...<br/>Year introduced: 2000(1989)
MeSH
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Alexander Disease
Alexander Disease
Rare leukoencephalopathy with infantile-onset accumulation of Rosenthal fibers in the subpial, periventricular, and subependymal zones of the brain. Rosenthal fibers are GLIAL...<br/>Year introduced: 2003
MeSH
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Friedreich Ataxia
Friedreich Ataxia
An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser exte...<br/>Year introduced: 2000(1966)
MeSH
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