Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood

Helle Highland Nygaard, David Gaist, Mette Christensen, Morten Dunø, Margrethe Kjeldsen, Henrik Daa Schrøder, Niels Gregersen, Flemming Wibrand, Rikke Katrine Jentoft Olsen, Jens Michael Hertz

Research output: Contribution to conference without publisher/journalConference abstract for conferenceResearch

Original languageEnglish
Publication date5. May 2016
Publication statusPublished - 5. May 2016
EventThe 18th Nordic Congress in Human Genetics: Nordic Congress in Clinical Laboratory Genetics - Harpa Conference Center, Reykjavik, Iceland
Duration: 5. May 20167. May 2016
Conference number: 18

Conference

ConferenceThe 18th Nordic Congress in Human Genetics
Number18
LocationHarpa Conference Center
CountryIceland
CityReykjavik
Period05/05/201607/05/2016

Cite this

Highland Nygaard, H., Gaist, D., Christensen, M., Dunø, M., Kjeldsen, M., Schrøder, H. D., ... Hertz, J. M. (2016). Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood. Abstract from The 18th Nordic Congress in Human Genetics, Reykjavik, Iceland.
Highland Nygaard, Helle ; Gaist, David ; Christensen, Mette ; Dunø, Morten ; Kjeldsen, Margrethe ; Schrøder, Henrik Daa ; Gregersen, Niels ; Wibrand, Flemming ; Olsen, Rikke Katrine Jentoft ; Hertz, Jens Michael. / Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood. Abstract from The 18th Nordic Congress in Human Genetics, Reykjavik, Iceland.
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title = "Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood",
author = "{Highland Nygaard}, Helle and David Gaist and Mette Christensen and Morten Dun{\o} and Margrethe Kjeldsen and Schr{\o}der, {Henrik Daa} and Niels Gregersen and Flemming Wibrand and Olsen, {Rikke Katrine Jentoft} and Hertz, {Jens Michael}",
year = "2016",
month = "5",
day = "5",
language = "English",
note = "null ; Conference date: 05-05-2016 Through 07-05-2016",

}

Highland Nygaard, H, Gaist, D, Christensen, M, Dunø, M, Kjeldsen, M, Schrøder, HD, Gregersen, N, Wibrand, F, Olsen, RKJ & Hertz, JM 2016, 'Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood', The 18th Nordic Congress in Human Genetics, Reykjavik, Iceland, 05/05/2016 - 07/05/2016.

Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood. / Highland Nygaard, Helle ; Gaist, David; Christensen, Mette; Dunø, Morten; Kjeldsen, Margrethe; Schrøder, Henrik Daa; Gregersen, Niels; Wibrand, Flemming; Olsen, Rikke Katrine Jentoft; Hertz, Jens Michael.

2016. Abstract from The 18th Nordic Congress in Human Genetics, Reykjavik, Iceland.

Research output: Contribution to conference without publisher/journalConference abstract for conferenceResearch

TY - ABST

T1 - Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood

AU - Highland Nygaard, Helle

AU - Gaist, David

AU - Christensen, Mette

AU - Dunø, Morten

AU - Kjeldsen, Margrethe

AU - Schrøder, Henrik Daa

AU - Gregersen, Niels

AU - Wibrand, Flemming

AU - Olsen, Rikke Katrine Jentoft

AU - Hertz, Jens Michael

PY - 2016/5/5

Y1 - 2016/5/5

M3 - Conference abstract for conference

ER -

Highland Nygaard H, Gaist D, Christensen M, Dunø M, Kjeldsen M, Schrøder HD et al. Isobutyryl-CoA Dehydrogenase Deficiency Presenting with Significant Clinical Disease in Adulthood. 2016. Abstract from The 18th Nordic Congress in Human Genetics, Reykjavik, Iceland.