Document Detail


Huntington's disease: testing the test.
MedLine Citation:
PMID:  8401575     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Authors:
A P Read
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Publication Detail:
Type:  Comment; News    
Journal Detail:
Title:  Nature genetics     Volume:  4     ISSN:  1061-4036     ISO Abbreviation:  Nat. Genet.     Publication Date:  1993 Aug 
Date Detail:
Created Date:  1993-11-05     Completed Date:  1993-11-05     Revised Date:  2005-11-17    
Medline Journal Info:
Nlm Unique ID:  9216904     Medline TA:  Nat Genet     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  329-30     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Base Sequence
Female
Fragile X Mental Retardation Protein
Fragile X Syndrome / genetics
Humans
Huntington Disease / diagnosis*,  genetics*
Male
Mutation*
Nerve Tissue Proteins / genetics
Pedigree
RNA-Binding Proteins*
Repetitive Sequences, Nucleic Acid
Chemical
Reg. No./Substance:
0/FMR1 protein, human; 0/Nerve Tissue Proteins; 0/RNA-Binding Proteins; 139135-51-6/Fragile X Mental Retardation Protein
Comments/Corrections
Comment On:
Nat Genet. 1993 Aug;4(4):398-403   [PMID:  8401589 ]
Nat Genet. 1993 Aug;4(4):393-7   [PMID:  8401588 ]
Nat Genet. 1993 Aug;4(4):387-92   [PMID:  8401587 ]

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