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Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype

Mario Lucariello; Enrique Vidal; Silvia Vidal; Mauricio Saez; Laura Roa; Dori Huertas; Mercè Pineda; Esther Dalfó; Joaquin Dopazo; Paola Jurado; Judith Armstrong; Manel Esteller
Human Genetics · Vol. 135, Issue 12 · pp. 1343-1354 · 2016

Abstract

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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2016-12-01
Publication Year2016
Volume135
Issue12
Pages1343-1354
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-016-1721-3

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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