Difference of new mutation rates in dystrophic gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy

Jun Kawamura, Shingo Kato, Tadayuki Ishihara, Yoshiyuki Hiraishi, Takeo Kawashiro

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

To clarify new mutational rates in the dystrophic gene between deletion and duplication mutations, carrier diagnosis wits performed on 123 mothers of probands suffered from Duchenne (DMD) and Becker (BMD) muscular dystrophy. Quantitative Southern blot analysis with cDNA probes was applied in this study. Out of 108 mothers of DMD/BMD patients with deletion mutation in dystrophic gene, 69 were carriers and 39 were non-carriers. On the other hands, all of 15 mothers of probands with duplication mutation were carriers. The fact that no new mutation occurred in oogenesis in the families with duplication mutations in dystrophin gene indicates that duplications arise in spermatogenesis. The risk of the mother of an isolated case of DMD/BMD with duplication mutation of being a carrier is significantly higher than the estimated risk based on the equality of new mutation in oogenesis and spermatogenesis.

Original languageEnglish
Pages (from-to)212-217
Number of pages6
JournalClinical Neurology
Volume37
Issue number3
Publication statusPublished - 1997 Mar

Fingerprint

Gene Duplication
Duchenne Muscular Dystrophy
Sequence Deletion
Gene Deletion
Mutation Rate
Mutation
Mothers
Oogenesis
Spermatogenesis
Dystrophin
Wit and Humor
Southern Blotting
Complementary DNA
Genes

Keywords

  • Deletion
  • Duchenne muscular dystrophy
  • Duplication
  • Dystrophic
  • New mutation

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Difference of new mutation rates in dystrophic gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy. / Kawamura, Jun; Kato, Shingo; Ishihara, Tadayuki; Hiraishi, Yoshiyuki; Kawashiro, Takeo.

In: Clinical Neurology, Vol. 37, No. 3, 03.1997, p. 212-217.

Research output: Contribution to journalArticle

Kawamura, J, Kato, S, Ishihara, T, Hiraishi, Y & Kawashiro, T 1997, 'Difference of new mutation rates in dystrophic gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy', Clinical Neurology, vol. 37, no. 3, pp. 212-217.
Kawamura, Jun ; Kato, Shingo ; Ishihara, Tadayuki ; Hiraishi, Yoshiyuki ; Kawashiro, Takeo. / Difference of new mutation rates in dystrophic gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy. In: Clinical Neurology. 1997 ; Vol. 37, No. 3. pp. 212-217.
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