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British Journal of Dermatology, ISSN 0007-0963, 11/2018, Volume 179, Issue 5, pp. 1210 - 1211
Journal Article
Turkiye Klinikleri Dermatoloji, ISSN 1300-0330, 12/2013, Volume 23, Issue 2, pp. 63 - 65
Journal Article
Human Mutation, ISSN 1059-7794, 10/2017, Volume 38, Issue 10, pp. 1355 - 1359
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 06/2018, Volume 35, Issue 3, pp. 366 - 370
Journal Article
Journal of Dermatological Science, ISSN 0923-1811, 07/2018, Volume 91, Issue 1, pp. 35 - 42
Background: Piebaldism is a pigmentary disorder characterized by a white forelock and depigmented patches. Although the loss-of-function mutations in the KIT... 
Heterodimerization | Piebaldism | Endoplasmic reticulum | KIT signaling | KIT gene
Journal Article
Journal of Dermatological Science, ISSN 0923-1811, 07/2018, Volume 91, Issue 1, pp. 35 - 42
Piebaldism is a pigmentary disorder characterized by a white forelock and depigmented patches. Although the loss-of-function mutations in the gene underlie the... 
Heterodimerization | Piebaldism | Endoplasmic reticulum | KIT signaling | KIT gene | Index Medicus
Journal Article
The Pan African medical journal, 2017, Volume 27, pp. 221 - 221
Piebaldism is a rare autosomal dominant genodermatosis. It is due to congenital absence of melanocytes in the affected areas. We report a case. A 5 year old... 
Diagnosis, Differential | Piebaldism - diagnosis | Piebaldism - genetics | Humans | Melanocytes - pathology | Child, Preschool | Female | Proto-Oncogene Proteins c-kit - genetics | Mutation | Piebaldism - pathology | Index Medicus
Journal Article
Journal Article
Revista Cubana de Pediatria, ISSN 0034-7531, 2014, Volume 86, Issue 1, pp. 93 - 97
Journal Article
Journal of Cutaneous Pathology, ISSN 0303-6987, 12/2018, Volume 45, Issue 12, pp. 918 - 922
Journal Article
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