Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair.

Abstract

American Journal of Medical Genetics Part AVolume 173, Issue 2 p. 565-567 Research Letter Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair Regina M. Zambrano, Corresponding Author Regina M. Zambrano rzambra1@jhmi.edu Division of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, Louisiana Corresponcence to: Dr. Regina Zambrano and Dr. Yves Lacassie, Divisions of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, 200 Henry Clay Avenue New Orleans, LA. E-mail: rzambra1@jhmi.edu (Y.L); ylacas@lsuhsc.edu (R.Z)Search for more papers by this authorMichael Marble, Michael Marble Division of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorStuart A. Chalew, Stuart A. Chalew Division of Endocrinology, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorChristian Lilje, Christian Lilje Division of Cardiology, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorAlfonso Vargas, Alfonso Vargas Division of Endocrinology, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorYves Lacassie, Corresponding Author Yves Lacassie ylacas@lsuhsc.edu Division of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, Louisiana Corresponcence to: Dr. Regina Zambrano and Dr. Yves Lacassie, Divisions of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, 200 Henry Clay Avenue New Orleans, LA. E-mail: rzambra1@jhmi.edu (Y.L); ylacas@lsuhsc.edu (R.Z)Search for more papers by this author Regina M. Zambrano, Corresponding Author Regina M. Zambrano rzambra1@jhmi.edu Division of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, Louisiana Corresponcence to: Dr. Regina Zambrano and Dr. Yves Lacassie, Divisions of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, 200 Henry Clay Avenue New Orleans, LA. E-mail: rzambra1@jhmi.edu (Y.L); ylacas@lsuhsc.edu (R.Z)Search for more papers by this authorMichael Marble, Michael Marble Division of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorStuart A. Chalew, Stuart A. Chalew Division of Endocrinology, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorChristian Lilje, Christian Lilje Division of Cardiology, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorAlfonso Vargas, Alfonso Vargas Division of Endocrinology, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, LouisianaSearch for more papers by this authorYves Lacassie, Corresponding Author Yves Lacassie ylacas@lsuhsc.edu Division of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, New Orleans, Louisiana Corresponcence to: Dr. Regina Zambrano and Dr. Yves Lacassie, Divisions of Genetics, Department of Pediatrics, Louisiana State University Health Sciences Center School of Medicine, and Children's Hospital, 200 Henry Clay Avenue New Orleans, LA. E-mail: rzambra1@jhmi.edu (Y.L); ylacas@lsuhsc.edu (R.Z)Search for more papers by this author First published: 21 November 2016 https://doi.org/10.1002/ajmg.a.38056Citations: 17 Conflict of interest: None. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume173, Issue2February 2017Pages 565-567 RelatedInformation