Emery-Dreifuss muscular dystrophy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/5200744.pdf
Reference28 articles.
1. Emery AEH . Emery-Dreifuss muscular dystrophy – a 40 year retrospective Neuromusc Disord 2000 10: 228–232
2. Bonne G, Mercuri E, Muchir A et al. Clinical and molecular genetic spectrum of autosomal dominant Emery Dreifuss muscular dystrophy due to mutations of the lamin A/C gene Ann Neurol 2000 48: 170–180
3. Sabatelli P, Squarzoni S, Petrini S et al. Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriers Neuromusc Disord 1998 8: 67–71
4. di Barletta MR, Ricci E, Galluzzi G et al. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy Am J Hum Genet 2000 66: 1407–1412
5. Bione S, Maestrini E, Rivella S et al. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy Nature Genet 1994 8: 323–327
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