Expansion of NEUROD2 phenotypes to include developmental delay without seizures.
Saved in:
| Title: | Expansion of NEUROD2 phenotypes to include developmental delay without seizures. |
|---|---|
| Authors: | Mis EK; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Sega AG; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Signer RH; Department of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California, USA., Cartwright T; Cortica, San Rafael, California, USA., Ji W; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Martinez-Agosto JA; Deparment of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, USA., Nelson SF; Department of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California, USA.; Deparment of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, USA.; Department of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, California, USA., Palmer CGS; Department of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California, USA.; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, USA.; Institute for Society and Genetics, University of California Los Angeles, Los Angeles, California, USA., Lee H; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, USA.; Department of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, California, USA., Mitzelfelt T; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Konstantino M; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Jeffries L; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Khokha MK; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Marco E; Cortica, San Rafael, California, USA.; Pediatric Brain Center, University of California San Francisco, San Francisco, California, USA., Martin MG; Deparment of Pediatrics, University of California Los Angeles, Los Angeles, California, USA., Lakhani SA; Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA. |
| Corporate Authors: | Undiagnosed Diseases Network |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2021 Apr; Vol. 185 (4), pp. 1076-1080. Date of Electronic Publication: 2021 Jan 13. |
| Publication Type: | Case Reports; Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
