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MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution
Authors
A Rett
Albert Nobre Menezes
+32 more
Alcides Pissinatti
B Langmead
CG Schrago
CM McGraw
CO Olson
F Ronquist
Héctor N. Seuánez
IM Buyse
J Singh
JM Dragich
JM Weitzel
JP Buschdorf
JW Alfaro
K Tamura
KA Aldinger
KC Hite
M Anisimova
Maria Carolina Viana
MD Shahbazian
Miguel Angelo M. Moreira
RE Amir
RJ Klose
RM Zachariah
RR Meehan
S Guindon
SW Long
TA Hall
TM Keane
VR Liyanage
W Delport
X Nan
X Nan
Publication date
Publisher
'Springer Science and Business Media LLC'
Doi
Abstract
Abstract is not available.
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info:doi/10.1186%2Fs12863-015-...
Last time updated on 05/06/2019
