Skip to content

Opening book details…

About this Medicine article

Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder with Skeletal Muscle Hypertrophy and Premature Cardiac Death by Xue, Yuan; Schoser, Benedikt; Rao, Aliz R.; Quadrelli, Roberto; Vaglio, Alicia; Rupp, Verena; Beichler, Christine; Nelson, Stanley F.; Schappacher-Tilp, Gudrun; Windpassinger, Christian; Wilcox, William R. is a Medicine article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Medicine.

Author
Xue, Yuan; Schoser, Benedikt; Rao, Aliz R.; Quadrelli, Roberto; Vaglio, Alicia; Rupp, Verena; Beichler, Christine; Nelson, Stanley F.; Schappacher-Tilp, Gudrun; Windpassinger, Christian; Wilcox, William R.
Publisher
Ovid Technologies Wolters Kluwer -American Heart Association; Lippincott Williams & Wilkins Ltd.; Ovid Technologies (Wolters Kluwer Health) (ISSN 1942-325X)
Published
2016
Language
EN
Field
Medicine (Life Sciences)

More by Xue, Yuan; Schoser, Benedikt; Rao, Aliz R.; Quadrelli, Roberto; Vaglio, Alicia; Rupp, Verena; Beichler, Christine; Nelson, Stanley F.; Schappacher-Tilp, Gudrun; Windpassinger, Christian; Wilcox, William R.

Browse all works by Xue, Yuan; Schoser, Benedikt; Rao, Aliz R.; Quadrelli, Roberto; Vaglio, Alicia; Rupp, Verena; Beichler, Christine; Nelson, Stanley F.; Schappacher-Tilp, Gudrun; Windpassinger, Christian; Wilcox, William R.