New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy

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Pysyväisosoite

http://hdl.handle.net/10138/285188

Lähdeviite

Moreau-Le Lan , S , Aller , E , Calabria , I , Gonzalez-Tarancon , L , Cardona-Gay , C , Martinez-Matilla , M , Aparisi , M J , Selles , J , Sagath , L , Pitarch , I , Muelas , N , Cervera , J V , Millan , J M & Pedrola , L 2018 , ' New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy ' , PLoS One , vol. 13 , no. 12 , 0207296 . https://doi.org/10.1371/journal.pone.0207296

Julkaisun nimi: New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy
Tekijä: Moreau-Le Lan, Sarah; Aller, Elena; Calabria, Ines; Gonzalez-Tarancon, Lola; Cardona-Gay, Cristina; Martinez-Matilla, Marina; Aparisi, Maria J.; Selles, Jorge; Sagath, Lydia; Pitarch, Inmaculada; Muelas, Nuria; Cervera, Jose V.; Millan, Jose M.; Pedrola, Laia
Tekijän organisaatio: Biosciences
Department of Medical and Clinical Genetics
Medicum
University of Helsinki
Päiväys: 2018-12-05
Kieli: eng
Sivumäärä: 12
Kuuluu julkaisusarjaan: PLoS One
ISSN: 1932-6203
DOI-tunniste: https://doi.org/10.1371/journal.pone.0207296
URI: http://hdl.handle.net/10138/285188
Tiivistelmä: Nemaline Myopathy (NM) is a rare genetic disorder that encompasses a large spectrum of myopathies characterized by hypotonia and generalized muscle weakness. To date, mutations in thirteen different genes have been associated with NM. The most frequently responsible genes are NEB (50% of cases) and ACTA1 (15-25% of cases). In this report all known NM related genes were screened by Next Generation Sequencing in five Spanish patients in order to genetically confirm the clinical and histological diagnosis of NM. Four mutations in NEB (c.17779_17780delTA, c.11086A>C, c.21076C>T and c.2310+5G>A) and one mutation in ACTA1 (c.871A>T) were found in four patients. Three of the four mutations in NEB were novel. A cDNA sequencing assay of the nove/variants c.17779_17780delTA, c.11086A>C and c.2310+5G>A revealed that the intronic variant c.2310+5G>A affected the splicing process. Mutations reported here could help clinicians and geneticists in NM diagnosis.
Avainsanat: NEBULIN
VARIANTS
3121 General medicine, internal medicine and other clinical medicine
Vertaisarvioitu: Kyllä
Tekijänoikeustiedot: cc_by
Pääsyrajoitteet: openAccess
Rinnakkaistallennettu versio: publishedVersion


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