Počet záznamů: 1
Phenotype-genotype correlations in patients with Marinesco-Sjogren syndrome
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SYSNO ASEP 0436676 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Phenotype-genotype correlations in patients with Marinesco-Sjogren syndrome Tvůrce(i) Ezgu, F. (US)
Krejčí, Pavel (BFU-R)
Li, S. (US)
de Sousa, P. (GB)Celkový počet autorů 12 Zdroj.dok. Clinical Genetics. - : Wiley - ISSN 0009-9163
Roč. 86, č. 1 (2014), s. 74-84Poč.str. 11 s. Forma vydání Tištěná - P Jazyk dok. eng - angličtina Země vyd. US - Spojené státy americké Klíč. slova BIP-associated protein ; endoplasmic reticulum stress ; Marinesco-Sjogren Syndrome Vědní obor RIV BO - Biofyzika Institucionální podpora BFU-R - RVO:68081707 UT WOS 000337538900011 DOI https://doi.org/10.1111/cge.12230 Anotace Marinesco-Sjogren syndrome (MSS; MIM 248800) is an autosomal recessive disorder characterized by congenital cerebellar ataxia, early cataracts, developmental delay, myopathy and short stature. Alterations in the gene SIL1 cause MSS in some patients with typical findings. In this study, molecular investigations including sequencing of the SIL1 gene, western blotting and microscopic investigations in fibroblast cultures were carried out in a cohort of 15 patients from 14 unrelated families, including the large, inbred family reported by Superneau et al., having the clinical features of MSS to provide insights into the pathophysiology of the disorder. A total of seven different mutations were found in eight of the patients from seven families. The mutations caused loss of the BIP-associated protein (BAP) protein in four patients by western blot. Novel clinical features such as dental abnormalities, iris coloboma, eczema and hormonal abnormalities were noticed in some patients, but there was no clear way to distinguish those with and without SIL1 mutations. Pracoviště Biofyzikální ústav Kontakt Jana Poláková, polakova@ibp.cz, Tel.: 541 517 244 Rok sběru 2015
Počet záznamů: 1