| Added by | standudu |
|---|---|
| Group name | EquipeCTCS |
| Item Type | Note |
| Note | The following values have no corresponding Zotero field: auth-address: Reference Center of Inherited Metabolic Diseases, University Paris Descartes, Hospital Necker Enfants Malades, APHP, Paris, France. Department of Biochemistry, Hospital Bicetre, Le Kremlin Bicetre, France. Department of Pediatric Radiology, University Paris Descartes, Hospital Necker Enfants Malades, Paris, France. Department of Molecular Genetics, CNRS UMR 5535, Montpellier, France. Reference Center of Inherited Metabolic Diseases, University Paris Descartes, Hospital Necker Enfants Malades, APHP, Paris, France; Department of Biochemistry, University Paris Descartes, Hospital Necker Enfants Malades, Paris, France. Paris-Sud University, CNRS-UMR8621, Genetics and Microbiology Institute, Orsay, France. Reference Center of Inherited Metabolic Diseases, University Paris Descartes, Hospital Necker Enfants Malades, APHP, Paris, France. Electronic address: pascale.delonlay@nck.aphp.fr. alt-title: Mitochondrion accession-num: 24462778 |
| Tags | _EndnoteXML import |
| Date Added | 2018/11/14 - 15:24:46 |
| Date Modified | 2018/11/14 - 15:24:46 |
| Parent item | Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiency |
Institut de Recherche en Cancérologie de
