Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 1981 Jul;33(4):513-8.

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21

Case Reports

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21

P A Jacobs et al. Am J Hum Genet. 1981 Jul.

Abstract

An isolated case of Duchenne muscular dystrophy in a female who has a de novo t(X;5)(p21;q35) translocation is described. The similarities between this patient and four previously reported females with Duchenne muscular dystrophy are discussed. It is concluded that the locus for Duchenne muscular dystrophy is at Xp21 and, furthermore, that this site may be particularly susceptible both to chromosome breakage and exchange and to gene mutation.

PubMed Disclaimer

References

    1. Am J Hum Genet. 1976 May;28(3):213-27 - PubMed
    1. J Med Genet. 1979 Oct;16(5):389-92 - PubMed
    1. J Med Genet. 1980 Jun;17(3):216-21 - PubMed
    1. Cytogenet Cell Genet. 1980;27(4):268 - PubMed

Publication types

LinkOut - more resources