Cover Image, Volume 40, Issue 3. Issue 3 (10th February 2019)

• Record Type: Journal Article
• Authors: Rehman, Atteeq U.; Najafi, Maryam; Kambouris, Marios; Al‐Gazali, Lihadh; Makrythanasis, Periklis; Rad, Abolfazl; Maroofian, Reza; Rajab, Anna; Stark, Zornitza; Hunter, Jill V.; Bakey, Zeineb; Tokita, Mari J.; He, Weimin; Vetrini, Francesco; Petersen, Andrea; Santoni, Federico A.; Hamamy, Hanan; Wu, Kaman; Al‐Jasmi, Fatma; Helmstädter, Martin; Arnold, Sebastian J.; Xia, Fan; Richmond, Christopher; Liu, Pengfei; Karimiani, Ehsan Ghayoor; Karami Madani, GholamReza; Lunke, Sebastian; El‐Shanti, Hatem; Eng, Christine M.; Antonarakis, Stylianos E.; Hertecant, Jozef; Walkiewicz, Magdalena; Yang, Yaping; Schmidts, Miriam;
• Is Part Of: Human mutation. Volume 40:Issue 3(2019)
• Page Start: i
• Page End: i
• Publication Date: 2019-02-10
• Subjects: Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.22892
• Languages: English
• ISSNs: 1059-7794

Abstract

Abstract : On the Front Cover : This cover image is based on the Rapid Communication Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function by Atteeq U. Rehman et al., Pages 267–280. DOI:10.1002/humu.23694 .