A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome
, , , , und
31. Dez. 2016
Über diesen Artikel
Artikel-Kategorie: Case Report
Online veröffentlicht: 31. Dez. 2016
Seitenbereich: 95 - 100
DOI: https://doi.org/10.1515/bjmg-2016-0043
Schlüsselwörter
© 2016 Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V
This article is distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Bakšienė, M
Center for Medical Genetics, Vilnius University Hospital Santariškių KlinikosVilnius, Lithuania
Department of Human and Medical Genetics, Vilnius UniversityVilnius, Lithuania
Benušienė, E
Center for Medical Genetics, Vilnius University Hospital Santariškių KlinikosVilnius, Lithuania
Department of Human and Medical Genetics, Vilnius UniversityVilnius, Lithuania
Morkūnienė, A
Center for Medical Genetics, Vilnius University Hospital Santariškių KlinikosVilnius, Lithuania
Department of Human and Medical Genetics, Vilnius UniversityVilnius, Lithuania
Ambrozaitytė, L
Center for Medical Genetics, Vilnius University Hospital Santariškių KlinikosVilnius, Lithuania
Department of Human and Medical Genetics, Vilnius UniversityVilnius, Lithuania
Utkus, A
Center for Medical Genetics, Vilnius University Hospital Santariškių KlinikosVilnius, Lithuania
Department of Human and Medical Genetics, Vilnius UniversityVilnius, Lithuania
Kučinskas, V
Center for Medical Genetics, Vilnius University Hospital Santariškių KlinikosVilnius, Lithuania
Department of Human and Medical Genetics, Vilnius UniversityVilnius, Lithuania