Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2021-07-01
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| Series: | Frontiers in Neurology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fneur.2021.711288/full |
| _version_ | 1819144074057220096 |
|---|---|
| author | Francesca Cogliati Francesca Forzano Silvia Russo |
| author_facet | Francesca Cogliati Francesca Forzano Silvia Russo |
| author_sort | Francesca Cogliati |
| collection | DOAJ |
| first_indexed | 2024-12-22T12:36:21Z |
| format | Article |
| id | doaj.art-96c789c819cc4c6c8d0acb91f3713e6a |
| institution | Directory Open Access Journal |
| issn | 1664-2295 |
| language | English |
| last_indexed | 2024-12-22T12:36:21Z |
| publishDate | 2021-07-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Neurology |
| spelling | doaj.art-96c789c819cc4c6c8d0acb91f3713e6a2022-12-21T18:25:33ZengFrontiers Media S.A.Frontiers in Neurology1664-22952021-07-011210.3389/fneur.2021.711288711288Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental DisordersFrancesca Cogliati0Francesca Forzano1Silvia Russo2Research Laboratory of Medical Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milan, ItalyClinical Genetics Department, Guy's & St Thomas' National Health System Foundation Trust, London, United KingdomResearch Laboratory of Medical Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milan, Italyhttps://www.frontiersin.org/articles/10.3389/fneur.2021.711288/fulloverlapping phenotypespleiotropy of a single genemicrocephalySETBP1 geneSETD5 geneMRD23 syndrome |
| spellingShingle | Francesca Cogliati Francesca Forzano Silvia Russo Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders Frontiers in Neurology overlapping phenotypes pleiotropy of a single gene microcephaly SETBP1 gene SETD5 gene MRD23 syndrome |
| title | Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders |
| title_full | Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders |
| title_fullStr | Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders |
| title_full_unstemmed | Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders |
| title_short | Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders |
| title_sort | editorial overlapping phenotypes and genetic heterogeneity of rare neurodevelopmental disorders |
| topic | overlapping phenotypes pleiotropy of a single gene microcephaly SETBP1 gene SETD5 gene MRD23 syndrome |
| url | https://www.frontiersin.org/articles/10.3389/fneur.2021.711288/full |
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