Clinical, neuroradiological, and molecular phenotyping of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations
- Resource Type
- Source
- Molecular Genetics and Metabolism. 132:iv
- Subject
Pathology medicine.medical_specialty Endocrinology business.industry Endocrinology, Diabetes and Metabolism Genetics Medicine Zellweger Spectrum business Molecular Biology Biochemistry - Language
- ISSN
- 1096-7192