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Volumn 20, Issue 2, 1997, Pages 122-124
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Trinucleotide repeat disorders
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Author keywords
[No Author keywords available]
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Indexed keywords
CEREBELLAR ATAXIA;
CONFERENCE PAPER;
DENTATORUBROPALLIDOLUYSIAN ATROPHY;
FRAGILE X SYNDROME;
FRIEDREICH ATAXIA;
GENE MUTATION;
GENETIC ANALYSIS;
HUMAN;
HUNTINGTON CHOREA;
INBORN ERROR OF METABOLISM;
KENNEDY DISEASE;
MACHADO JOSEPH DISEASE;
MOLECULAR CLONING;
MYOTONIC DYSTROPHY;
SPINAL MUSCULAR ATROPHY;
TRINUCLEOTIDE REPEAT;
FRAGILE X SYNDROME;
HUMANS;
HUNTINGTON DISEASE;
METABOLIC DISEASES;
MUSCULAR ATROPHY, SPINAL;
MYOTONIC DYSTROPHY;
TRINUCLEOTIDE REPEATS;
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EID: 0030911169
PISSN: 01418955
EISSN: None
Source Type: Journal
DOI: 10.1023/A:1005388218625 Document Type: Conference Paper |
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Times cited : (6)
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References (0)
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