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Erratum to “Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome”, Am J Med Genet Part A 161A:1638–1646
Author(s) -
Chapleau Christopher A.,
Lane Jane,
Kirwin Susan,
Schanen Carolyn,
Vinette Kathy M. B.,
Stubbolo Danielle,
MacLeod Patrick,
Glaze Daniel G.,
Motil Kathleen J.,
Neul Jeffrey L.,
Skinner Steven A.,
Kaufmann Walter E.,
Percy Alan K.
Publication year - 2014
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.36493
Subject(s) - rett syndrome , mecp2 , gene , genetics , computational biology , biology , phenotype
© 2014 Wiley Periodicals, Inc.