Open AccessMice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome
Author(s) -
Dag H. Yasui,
M. L. Gonzales,
J. O. Aflatooni,
F. K. Crary,
D. J. Hu,
B. J. Gavino,
M. S. Golub,
John B. Vincent,
N. C. Schanen,
Carl O. Olson,
Mojgan Rastegar,
Janine M. LaSalle
Publication year - 2014
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddu496
Subject(s) - rett syndrome , biology , mecp2 , exon , mutation , gene isoform , genetics , phenotype , gene
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