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100301s2006 gw | s |||| 0|eng d |
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|a 9783540333364
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024 |
7 |
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|a 10.1007/3-540-33336-3
|2 doi
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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245 |
1 |
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|a Human Nucleotide Expansion Disorders /
|c edited by Michael Fry, Karen Usdin.
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250 |
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|a 1st ed. 2006.
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260 |
# |
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|a Berlin, Heidelberg :
|b Springer Berlin Heidelberg :
|b Imprint: Springer,
|c 2006.
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300 |
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|a XVIII, 294 p. :
|b online resource.
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336 |
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|a text
|b txt
|2 rdacontent
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337 |
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|a computer
|b c
|2 rdamedia
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338 |
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|a online resource
|b cr
|2 rdacarrier
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490 |
1 |
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|a Nucleic Acids and Molecular Biology,
|v 19
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505 |
0 |
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|a Molecular Bases of Nucleotide Expansions -- Mechanisms of DNA Repeat Expansion -- Disorders Associated with Non-coding Repeats -- Molecular Correlates of Fragile X Syndrome and FXTAS -- The Neglected Fragile X Mutations: FRAXE and FRAXF -- Friedreich Ataxia -- Dodecamer Repeat Expansion in Progressive Myoclonus Epilepsy 1 -- Myotonic Dystrophies Types 1 and 2 -- Spinocerebellar Ataxia Type 8 -- Recent Progress in Spinocerebellar Ataxia Type 10 -- Disorders Associated with Coding Repeats -- Polyglutamine Diseases -- The Enigma of Spinocerebellar Ataxia Type 6 -- Disorders Associated with Repeats in an Undetermined Location -- Spinocerebellar Ataxia Type 12 and Huntington’s Disease-Like 2: Clues to Pathogenesis -- Postscript -- Current Issues and Therapeutic Prospects.
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650 |
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|a Neurobiology.
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650 |
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|a Neurosciences.
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650 |
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|a Human genetics.
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650 |
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|a Cell biology.
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650 |
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|a Biochemistry.
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650 |
1 |
4 |
|a Neurobiology.
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650 |
2 |
4 |
|a Neurosciences.
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650 |
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4 |
|a Human Genetics.
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650 |
2 |
4 |
|a Cell Biology.
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650 |
2 |
4 |
|a Biochemistry, general.
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700 |
1 |
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|a Fry, Michael.
|e editor.
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700 |
1 |
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|a Usdin, Karen.
|e editor.
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710 |
2 |
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|a SpringerLink (Online service)
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773 |
0 |
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|t Springer eBooks
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