An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2004.01060.x/fullpdf
Reference11 articles.
1. Long-term Follow-up of Facioscapulohumeral Muscular Dystrophy and Coats' Disease
2. RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY
3. Inappropriate Gene Activation in FSHD
4. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
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1. Leber Mitochondrial Optic Neuropathy in Pediatric Females With Focus on Very Early Onset Cases;Journal of Child Neurology;2023-01-19
2. The epidemiology and mutation types of Leber’s hereditary optic neuropathy in Thailand;Annals of Medicine;2022-06-06
3. Optic Atrophy in Children;Pediatric Neuro-Ophthalmology;2016
4. Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears;Current Molecular Medicine;2014-10-13
5. Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes;BMC Medical Genetics;2013-09-16
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