MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases-Reference-Cited by-同舟云学术

MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases

Published:2018-05-21 Issue:7 Volume:39 Page:914-924
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Townend Gillian S.¹^ORCID,Ehrhart Friederike¹²^ORCID,van Kranen Henk J.¹³^ORCID,Wilkinson Mark⁴^ORCID,Jacobsen Annika⁵^ORCID,Roos Marco⁵^ORCID,Willighagen Egon L.²,van Enckevort David⁶^ORCID,Evelo Chris T.¹²^ORCID,Curfs Leopold M. G.¹^ORCID

Affiliation:

1. Rett Expertise Centre Netherlands - GKC; Maastricht University Medical Center; Maastricht The Netherlands

2. Department of Bioinformatics - BiGCaT; NUTRIM; Maastricht University; Maastricht The Netherlands

3. Institute for Public Health Genomics; Maastricht University; Maastricht The Netherlands

4. Center for Plant Biotechnology and Genomics; Universidad Politécnica de Madrid; Madrid Spain

5. Department of Human Genetics; Leiden University Medical Center; Leiden The Netherlands

6. Department of Genetics; University Medical Center Groningen; University of Groningen; Groningen The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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