A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome
By: M Bakšienė, E Benušienė, A Morkūnienė, L Ambrozaitytė, A Utkus and V Kučinskas
DOI: https://doi.org/10.1515/bjmg-2016-0043 | Journal eISSN: 2199-5761
Language: English
Page range: 95 - 100
Published on: Dec 31, 2016
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2016 M Bakšienė, E Benušienė, A Morkūnienė, L Ambrozaitytė, A Utkus, V Kučinskas, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.