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Autori: Hahn Andreas

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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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 
Info NEUROMUSCULAR DISORDERS, (2016), vol. 26 br. , Suppl. 2, str. S108-S109
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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