Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder.
Saved in:
| Title: | Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder. |
|---|---|
| Authors: | Liaqat K; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA., Treat K; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA., Wilson TE; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Conboy E; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA., Vetrini F; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA. |
| Source: | Clinical genetics [Clin Genet] 2024 Apr; Vol. 105 (4), pp. 455-456. Date of Electronic Publication: 2024 Feb 12. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| 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.
Login for full access.
|
|
| ISSN: | 1399-0004 |
|---|---|
| DOI: | 10.1111/cge.14497 |