trinucleotide repeat disorder
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Trinucleotide repeat disorder — Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation … Wikipedia
Trinucleotide repeat expansion — Trinucleotide repeat expansion= Trinucleotide repeat expansion, also known as triplet repeat expansion, is the DNA mutation responsible for causing any type of disorder categorized as a trinucleotide repeat disorder. These are labelled in… … Wikipedia
trinucleotide repeat — triplet repeat an unstable DNA sequence of three nucleotides, occurring in some human genes and normally repeated in tandem 5 to 50 times; expansion above that number has been linked to certain genetic disorders. The triplet sequences always… … Medical dictionary
Myotonic dystrophy — Classification and external resources ICD 10 G71.1 OMIM 160900 602668 … Wikipedia
Neurodegeneration — Classification and external resources Para sagittal MRI of the head in a patient with benign familial macrocephaly. ICD 10 G30 G32 … Wikipedia
ATN1 — is a protein found in nervous tissue.It is associated with a form of trinucleotide repeat disorder known as dentatorubral pallidoluysian atrophy or dentatorubropallidoluysian atrophy . PBB Summary section title = summary text = Dentatorubral… … Wikipedia
Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH … Wikipedia
Eukaryotic chromosome fine structure — refers to the structure of sequences for eukaryotic chromosomes. Some fine sequences are included in more than one class, so the classification listed is not intended to be completely separate.Chromosomal characteristicsSome sequences are… … Wikipedia
Frataxin — is a small protein, localized to the mitochondrion. The function of frataxin is not entirely clear, but it seems to be involved in assembly of iron sulfur clusters.Deficiency of frataxin is the cause of Friedrich s ataxia, a hereditary… … Wikipedia
Oculopharyngeal muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 … Wikipedia
