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A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome

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31 dic 2016
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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
Lingua:
Inglese
Frequenza di pubblicazione:
2 volte all'anno
Argomenti della rivista:
Medicina, Scienze medicali di base, Scienze medicali di base, altro