Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts-Reference-Cited by-同舟云学术

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Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts

Published:1997-07 Issue:7 Volume:79 Page:439-448
ISSN:0300-9084
Container-title:Biochimie
language:en
Short-container-title:Biochimie

Author:

Kwiatkowska J.,Lisiecka D.,Sowinska J.,Marszal E.,Emich-Widera E.,Ciesielski T.,Szczególa-Przymusiak A.,Nuc P.,Chlebowska H.,Zimowski J.,Galas-Zgorzalewicz B.,Slonski R.

Publisher

Elsevier BV

Subject

General Medicine,Biochemistry

Reference41 articles.

1. Population frequencies of inherited neuromuscular diseases a world survey;Emery;Neuromuscular Disorders,1991

2. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig;Cell,1987

3. The complete sequence of dystrophin predicts a rodshaped cytoskeletal protein;Koenig;Cell,1988

4. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den Dunnen;Am J Hum Genet,1989

5. Mendelian inheritance in man;McKusick,1990

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1. Comparative-high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations;Human Genetics;2013-11-15

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