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Pregled bibliografske jedinice broj: 284016

Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1


Boor, Ilja P.K.; de Groot, K.; Mejaški-Bošnjak, Vlatka; Brenner, C.; van der Knaap, M.S.; Scheper, G.C.; Pronk, J.C.
Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1 // Human Mutation, 27 (2006), 6; 505-512 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 284016 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1

Autori
Boor, Ilja P.K. ; de Groot, K. ; Mejaški-Bošnjak, Vlatka ; Brenner, C. ; van der Knaap, M.S. ; Scheper, G.C. ; Pronk, J.C.

Izvornik
Human Mutation (1059-7794) 27 (2006), 6; 505-512

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
megalencephalic leukoencephalopathy; subcortical cysts; MLC mutation

Sažetak
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is an autosomal recessive cerebral white matter disorder in children. This disease is histopathologically characterized by myelin splitting and intramyelinic vacuole formation. MLC is caused by mutations in the gene MLC1, which encodes a novel protein, MLC1. Since the first report, 50 mutations in this gene have been found. Mutations occur throughout the entire coding region and include all different types: 11 splice-site mutations ; one nonsense mutation ; 24 missense mutations ; and 14 deletions and insertions. Until now, six polymorphisms within the coding sequence of MLC1 had been reported. In about 20% of the patients with a typical clinical and MRI picture, no mutations in the MLC1 gene are found. Several of the families, in which no mutations are found, also do not show linkage with the MLC1 locus, which suggests a second gene involved in MLC. The absence of mutations may also be the consequence of performing standard mutation analysis that can miss heterozygous deletions, mutations in the promoter, 3' and 5' untranslated regions (UTRs), and intron mutations, which may influence the amino acid composition of the end product. In this work we describe 13 novel mutations, including those found with extended mutation analysis on MLC patients. This study shows that extended mutation analysis is a valuable tool to identify at least some of the missing mutations. Therefore, we suggest extended mutation analysis for the MLC1 gene, if no mutations are found during standard analysis.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekti:
0072002

Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta

Profili:

Avatar Url Vlatka Mejaški-Bošnjak (autor)


Citiraj ovu publikaciju:

Boor, Ilja P.K.; de Groot, K.; Mejaški-Bošnjak, Vlatka; Brenner, C.; van der Knaap, M.S.; Scheper, G.C.; Pronk, J.C.
Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1 // Human Mutation, 27 (2006), 6; 505-512 (međunarodna recenzija, članak, znanstveni)
Boor, I., de Groot, K., Mejaški-Bošnjak, V., Brenner, C., van der Knaap, M., Scheper, G. & Pronk, J. (2006) Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1. Human Mutation, 27 (6), 505-512.
@article{article, author = {Boor, Ilja P.K. and de Groot, K. and Meja\v{s}ki-Bo\v{s}njak, Vlatka and Brenner, C. and van der Knaap, M.S. and Scheper, G.C. and Pronk, J.C.}, year = {2006}, pages = {505-512}, keywords = {megalencephalic leukoencephalopathy, subcortical cysts, MLC mutation}, journal = {Human Mutation}, volume = {27}, number = {6}, issn = {1059-7794}, title = {Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1}, keyword = {megalencephalic leukoencephalopathy, subcortical cysts, MLC mutation} }
@article{article, author = {Boor, Ilja P.K. and de Groot, K. and Meja\v{s}ki-Bo\v{s}njak, Vlatka and Brenner, C. and van der Knaap, M.S. and Scheper, G.C. and Pronk, J.C.}, year = {2006}, pages = {505-512}, keywords = {megalencephalic leukoencephalopathy, subcortical cysts, MLC mutation}, journal = {Human Mutation}, volume = {27}, number = {6}, issn = {1059-7794}, title = {Megalencephallic leukoencephalopathy with subcortical cysts: An update and extended mutation analysis of MLC1}, keyword = {megalencephalic leukoencephalopathy, subcortical cysts, MLC mutation} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Uključenost u ostale bibliografske baze podataka::


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  • Biotechnology Citation Index&#8482
  • Cambridge Scientific Abstracts
  • Current Awareness in Biological Sciences
  • Current Opinion in Genetics & Development
  • Science Citation Index&#174
  • Science Citation Index Expanded&#8482
  • SCOPUS





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