Autori: Hahn Andreas
| Naslov | Strategies to shorten diagnostic delays for late infantile neuronal ceroid lipofuscinosis type 2 (CLN2 disease) (Meeting Abstract) |
| Autori | Mazurkiewicz-Beldinska Maria Del Toro Mireia Hahn Andreas Haliloglu Goknur Huidekop Hidde Kravljanac Ruzica M Muhlhausen Chris Andersen Brian Nauheimer Prpic Igor Striano Pasquale Auvin Stephane |
| Info | MOLECULAR GENETICS AND METABOLISM, (2020), vol. 129 br. 2, str. S106-S107 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations (Meeting Abstract) |
| Autori | Johnson Katherine Bertoli M Phillips L Toepf A Claeys K Rakocevic-Stojanovic Vidosava M Peric Stojan Z  Vissine J Hahn Andreas Maddison P Akay E Bastian A Lusakowska A Lek M Xu L MacArthur D Straub V
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| Info | NEUROMUSCULAR DISORDERS, (2016), vol. 26 br. , Suppl. 2, str. S108-S109 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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