Neuroscience and Neurosurgery in Southeast Europe
Author:
Affiliation:
1. School of Medicine, University of Belgrade, Beograd , Serbia
Publisher
Walter de Gruyter GmbH
Subject
General Medicine
Reference40 articles.
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3. 3. Hantke J, Chandler D, King R, Wanders RJ, Angelicheva D, Tournev I, et al. A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR). Eur J Hum Genet. 2009;17(12):1606-14.
4. 4. Todorova A, Litvinenko I, Todorov T, Tincheva R, Avdjieva D, Tincheva S, et al. A family with fragile X syndrome, Duchenne muscular dystrophy and ichthyosis transmitted by an asymptomatic carrier. Clin Genet. 2014;85(3):286-9.
5. 5. Litvinenko I, Kirov AV, Georgieva R, Todorov T, Malinova Z, Mitev V, et al. One Novel and One Recurrent Mutation in IGHMBP2 Gene, Causing Severe Spinal Muscular Atrophy Respiratory Distress 1 With Onset Soon After Birth. J Child Neurol. 2013;29(6):799-802.
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