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- Title
Correction to: 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces.
- Authors
Grünert, Sarah C.; Sass, Jörn Oliver
- Abstract
Seizures were reported in 13 patients The paragraph on the neurological outcome on page 3 also contains one wrong number and should read "Information on the neurologic outcome was available on 140 patients (Fig. 61.9% of patients show normal development, while severe mental disability is rather rare in this patient cohort. One 2-year-old patient had trisomy 21 [25] and was therefore not included in the analysis.
- Subjects
DEFICIENCY diseases; CEREBELLAR ataxia; DISABILITIES
- Publication
Orphanet Journal of Rare Diseases, 2022, Vol 17, Issue 1, p1
- ISSN
1750-1172
- Publication type
Journal Article
- DOI
10.1186/s13023-021-02154-z