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Ocular muscular dystrophy journal articles from PubMed MEDLINE database

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Chiara Manzini M, Gleason D, Chang BS, et al. 
Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East. [JOURNAL ARTICLE]
Hum Mutat 2008 Aug 27.
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Gál A, Szabó A, Pentelényi K, et al. 
[Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA.] [English Abstract, Journal Article]
Orv Hetil 2008 Aug 24; 149(34):1593-8.
Abstract | Full Citation
Moore CJ, Goh HT, Hewitt JE 
Genes required for functional glycosylation of dystroglycan are conserved in zebrafish. [JOURNAL ARTICLE]
Genomics 2008 Jul 14.
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Guo HM, Dong JK, Wang HM, et al. 
[Observation on therapeutic effect of acupuncture combined with western medicine on paralytic strabismus] [English Abstract, Journal Article]
Zhongguo Zhen Jiu 2008 Jun; 28(6):399-401.
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Cardaioli E, Da Pozzo P, Malfatti E, et al. 
Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNA. [JOURNAL ARTICLE]
J Neurol Sci 2008 Jul 4.
Abstract | Full Citation
Messina S, Mora M, Pegoraro E, et al. 
POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study. [JOURNAL ARTICLE]
Neuromuscul Disord 2008 May 29.
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Pérez Riera AR, Kaiser E, Levine P, et al. 
Kearns-Sayre syndrome: electro-vectorcardiographic evolution for left septal fascicular block of the his bundle. [JOURNAL ARTICLE]
J Electrocardiol 2008 May 17.
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Rose LV, Rose NT, Elder JE, et al. 
Ophthalmologic presentation of oxidative phosphorylation diseases of childhood. [Journal Article]
Pediatr Neurol 2008 Jun; 38(6):395-7.
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Rosen N 
Headache and mitochondrial disorders. [Journal Article]
Headache 2008 May; 48(5):733-4.
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Berio A, Oliaro E, Piazzi A 
Kearns-Sayre syndrome with corneal dystrophy, hypomagnesemia, GH deficiency, and reduced visual acuity. [Journal Article]
Panminerva Med 2008 Mar; 50(1):83-4.
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