about
Population genetic relationships between Mediterranean populations determined by HLA allele distribution and a historic perspectiveThe structural basis of myotonic dystrophy from the crystal structure of CUG repeatsExpression of a novel human myotonin protein kinase (MtPK) cDNA clone which encodes a protein with a thymopoietin-like domain in COS cells.Ocular motor myotonic phenomenon in myotonic dystrophy.CAG trinucleotide RNA repeats interact with RNA-binding proteins.Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testing.Prolonged Corrected QT Interval in Patients with Myotonic Dystrophy Type 1.A newly-described myotonic disorder (proximal myotonic myopathy--PROMM): personal experience and review of the literature.The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeat.Huntington disease: DNA analysis in Brazilian population.Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells.High conservation of the trinucleotide [CTG]n repeat at the myotonic dystrophy locus in nonhuman primates
P2860
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P2860
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
The myotonic dystrophy gene.
@en
type
label
The myotonic dystrophy gene.
@en
prefLabel
The myotonic dystrophy gene.
@en
P2093
P1433
P1476
The myotonic dystrophy gene.
@en
P2093
P304
P356
10.1001/ARCHNEUR.1993.00540110053005
P577
1993-11-01T00:00:00Z