Detection of a rare mutation in a Noonan syndrome suspected patient
Noonan syndrome (NS) is a genetic autosomal dominant condition, caused by mutations in PTPN11 and other genes. The aim of this report is to highlight a finding of a rare mutation in the RAF1 gene in a six-year-old child evaluated for Noonan Syndrome. An Ampliseq Research Panel covering A2ML1, BRAF,...
| Permalink: | http://skupnikatalog.nsk.hr/Record/nsk.NSK01001122404/Details |
|---|---|
| Matična publikacija: |
Molecular and experimental biology in medicine 3 (2020), 1 ; str. 44-47 |
| Glavni autori: | Dobrevski, Boban (Author), Shukarova Angelovska, Elena, Kirijas, Meri, Milanovski, Gorjan, Brnjarchevska Blazhevska, Teodora, Boceska, Frosina, Petlichkovski, Aleksandar |
| Vrsta građe: | e-članak |
| Jezik: | eng |
| Predmet: | |
| Online pristup: |
https://doi.org/10.33602/mebm.3.1.7 Molecular and experimental biology in medicine Hrčak |
| LEADER | 02461naa a22004334i 4500 | ||
|---|---|---|---|
| 001 | NSK01001122404 | ||
| 003 | HR-ZaNSK | ||
| 005 | 20220131101402.0 | ||
| 006 | m d | ||
| 007 | cr|||||||||||| | ||
| 008 | 211228s2020 ci d |o |0|| ||eng | ||
| 024 | 7 | |2 doi |a 10.33602/mebm.3.1.7 | |
| 035 | |a (HR-ZaNSK)001122404 | ||
| 040 | |a HR-ZaNSK |b hrv |c HR-ZaNSK |e ppiak | ||
| 041 | 0 | |a eng |b eng | |
| 042 | |a croatica | ||
| 044 | |a ci |c hr | ||
| 080 | 1 | |a 575 |2 2011 | |
| 100 | 1 | |a Dobrevski, Boban |4 aut |9 HR-ZaNSK | |
| 245 | 1 | 0 | |a Detection of a rare mutation in a Noonan syndrome suspected patient |h [Elektronička građa] : |b a case report / |c Boban Dobrevski, Elena Shukarova Angelovska, Meri Kirijas, Gorjan Milanovski, Teodora Brnjarchevska Blazhevska, Frosina Boceska, Aleksandar Petlichkovski. |
| 300 | |b Graf. prikazi. | ||
| 504 | |a Bibliografija: 15 jed. | ||
| 504 | |a Abstract. | ||
| 520 | |a Noonan syndrome (NS) is a genetic autosomal dominant condition, caused by mutations in PTPN11 and other genes. The aim of this report is to highlight a finding of a rare mutation in the RAF1 gene in a six-year-old child evaluated for Noonan Syndrome. An Ampliseq Research Panel covering A2ML1, BRAF, CBL, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RAF1, RIT1, SHOC2, SOS1 and SPRED1 genes was used on the Ion Torrent platform. Out of 54 variants detected, a single nucleotide missense mutation c.483T>G in the RAF1 gene was classified as likely pathogenic, based on a single previous submission to Clinvar. Further investigations may shed light on the possible role of this variant in the pathogenesis of Noonan Syndrome and other RASopathies. | ||
| 653 | 0 | |a Noonan sindrom |a Genetske bolesti |a Mutacije gena | |
| 653 | 6 | |a Prikaz slučaja | |
| 700 | 1 | |a Shukarova Angelovska, Elena |4 aut |9 HR-ZaNSK | |
| 700 | 1 | |a Kirijas, Meri |4 aut |9 HR-ZaNSK | |
| 700 | 1 | |a Milanovski, Gorjan |4 aut |9 HR-ZaNSK | |
| 700 | 1 | |a Brnjarchevska Blazhevska, Teodora |4 aut |9 HR-ZaNSK | |
| 700 | 1 | |a Boceska, Frosina |4 aut |9 HR-ZaNSK | |
| 700 | 1 | |a Petlichkovski, Aleksandar |4 aut | |
| 773 | 0 | |t Molecular and experimental biology in medicine |x 2584-671X |g 3 (2020), 1 ; str. 44-47 |w nsk.(HR-ZaNSK)000985906 | |
| 981 | |b Be2020 |b B04/20 | ||
| 998 | |b tino2201 | ||
| 856 | 4 | 0 | |u https://doi.org/10.33602/mebm.3.1.7 |
| 856 | 4 | 0 | |u http://www.mebm.eu/index.php/journal/article/view/63 |y Molecular and experimental biology in medicine |
| 856 | 4 | 0 | |u https://hrcak.srce.hr/238482 |y Hrčak |
| 856 | 4 | 1 | |y Digitalna.nsk.hr |