Email this article Brain function in Duchenne muscular dystrophy (Brain. — 2002. — Jan. — Vol. 125 (Pt 1). — P. 4—13: англ.)
- Authors: Anderson J.1, Head S.1, Rae C.1, Morley J.1
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Affiliations:
- University of New South Wales
- Issue: Vol XXXIV, No 1-2 (2002)
- Pages: 84-85
- Section: Abstracts
- URL: https://journals.rcsi.science/1027-4898/article/view/87587
- DOI: https://doi.org/10.17816/nb87587
- ID: 87587
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Abstract
Duchenne muscular dystrophy is the second most common genetic disorder in humans. The type of inheritance is recessive, linked to the X chromosome, the population frequency is one in 3300 newborn boys.
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##article.viewOnOriginalSite##About the authors
J. Anderson
University of New South Wales
Author for correspondence.
Email: info@eco-vector.com
School of Physiology and Pharmacology
Australia, SydneyS. Head
University of New South Wales
Email: info@eco-vector.com
School of Physiology and Pharmacology
Australia, SydneyC. Rae
University of New South Wales
Email: info@eco-vector.com
School of Physiology and Pharmacology
Australia, SydneyJ. Morley
University of New South Wales
Email: info@eco-vector.com
School of Physiology and Pharmacology
Australia, SydneyReferences
