Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity-Reference-Cited by-同舟云学术

Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity

Published:2009-06 Issue:6 Volume:50 Page:1612-1615
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Kecmanović Miljana,Ristić Aleksandar J.,Sokić Dragoslav,Keckarević-Marković Milica,Vojvodić Nikola,Ercegovac Marko,Janković Slavko,Keckarević Dušan,Savić-Pavićević Dušanka,Romac Stanka

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2008.01937.x/fullpdf

Reference13 articles.

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2. Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3;Bonne-Tamir;Am J Hum Genet,1996

3. Unstable insertion in the 5′ flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1;Lafrenière;Nat Genet,1997

4. Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy;Lalioti;Nature,1997

5. Familial myoclonus epilepsy associated with deaf-mutism in a family showing other psychobiological abnormalities;Latham;Ann Eugen,1937

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Shared Haplotype Indicates a Founder Event in Unverricht–Lundborg Disease Patients from Serbia;International Journal of Neuroscience;2013-09-12

2. Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygousCSTBpoint and indel mutations;Epilepsia;2012-12