Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome. Issue 5 (2nd May 2017)

Record Type:: Journal Article
Title:: Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome. Issue 5 (2nd May 2017)
Main Title:: Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome
Authors:: Bellusci, M.
Quijada‐Fraile, P.
Barrio‐Carreras, D.
Martin‐Hernandez, E.
Garcia‐Silva, M.
Merinero, B.
Perez, B.
Hernandez‐Lain, A.
Abstract:
Is Part Of:: Journal of inherited metabolic disease. Volume 40:Issue 5(2017)
Journal:: Journal of inherited metabolic disease
Issue:: Volume 40:Issue 5(2017)
Issue Display:: Volume 40, Issue 5 (2017)
Year:: 2017
Volume:: 40
Issue:: 5
Issue Sort Value:: 2017-0040-0005-0000
Page Start:: 751
Page End:: 752
Publication Date:: 2017-05-02
Subjects:: Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042
Journal URLs:: http://www.springer.com/gb/ ↗
DOI:: 10.1007/s10545-017-0041-7 ↗
Languages:: English
ISSNs:: 0141-8955
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 5006.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 10148.xml