Description |
1 online resource (xvii, 293 pages) : illustrations |
Series |
Nucleic acids and molecular biology, 0933-1891 ; 19 |
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Nucleic acids and molecular biology ; v. 19.
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Contents |
pt. I. Molecular bases of nucleotide expansions -- pt. II. Disorders associated with non-coding repeats -- pt. III. Disorders associated with coding repeats -- pt. IV. Disorders associated with repeats in an undetermined location -- pt. V. Postscript |
Summary |
Human neurological and neuromuscular disorders caused by nucleotide expansion, first discovered in 1991, are the focus of growing interest of practicing physicians and biomedical researchers. Useful to geneticists, molecular biologists, neurologists and pediatricians, this volume presents a description of many of the better-studied disorders |
Analysis |
biochemie |
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biochemistry |
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celbiologie |
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cellular biology |
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humane ziekten |
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human diseases |
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humane genetica |
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human genetics |
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neurobiologie |
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neurobiology |
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neurowetenschap |
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neuroscience |
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Medicine (General) |
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Geneeskunde (algemeen) |
Bibliography |
Includes bibliographical references and index |
Notes |
Print version record |
In |
Springer e-books |
Subject |
Nucleotide sequence.
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Medical genetics.
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Nervous system -- Diseases.
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Nucleotides.
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Biochemistry.
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Nervous System Diseases
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Genetics, Medical
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Nucleotides
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Biochemistry
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biochemistry.
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HEALTH & FITNESS -- Diseases -- Genetic.
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MEDICAL -- Genetics.
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Biomédecine.
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Sciences de la vie.
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Nucleotides
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Nervous system -- Diseases
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Medical genetics
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Nucleotide sequence
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Genmutation
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Repeats
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Erbkrankheit
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Form |
Electronic book
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Author |
Fry, Michael, Ph.D.
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Usdin, Karen.
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LC no. |
2006927799 |
ISBN |
9783540333364 |
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3540333363 |
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9783540333357 |
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3540333355 |
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