Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy.

Saved in:
Bibliographic Details
Title: Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy.
Authors: Leeuwen L; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Lubout CMA; Department of Pediatrics, Section of Metabolic Diseases, University of Groningen, Groningen, The Netherlands., Nijenhuis HP; Department of Pediatrics, Center for Congenital Heart Diseases, University of Groningen, Groningen, The Netherlands., Meiners LC; Department of Radiology, University of Groningen, Groningen, The Netherlands., Vos YJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Herkert JC; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Source: Clinical genetics [Clin Genet] 2022 Oct; Vol. 102 (4), pp. 350-351. Date of Electronic Publication: 2022 Jul 06.
Publication Type: Case Reports; Letter
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
Description
ISSN:1399-0004
DOI:10.1111/cge.14182