MECP2 variation in Rett syndrome - an...

Human Mutation 2018 / 04

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

Townend, Gillian S., Ehrhart, Friederike, van Kranen, Henk J., Wilkinson, Mark, Jacobsen, Annika, Roos, Marco, Willighagen, Egon L., van Enckevort, David, Evelo, Chris T., Curfs, Leopold M. G.
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Language:
english
Journal:
Human Mutation
DOI:
10.1002/humu.23542
Date:
April, 2018
File:
PDF, 680 KB
english, 2018
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