Molecular Basis of Human Piebaldism.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
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2. Familial white skin spotting (piebaldness) (“partial albinism”) with white forelock
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4. Some Account of a Motley Coloured, or Pye Negro Girl and Mulatto Boy, Exhibited before the Society in the Month of May, 1784, for Their Examination, by Dr. John Morgan, from the History Given of Them by Their Owner Mons. Le Vallois, Dentist of the King of France at Guadaloupe in the West Indies
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2. A novel mutation of the KIT gene in a Chinese family with piebaldism;Chinese Medical Journal;2013-06-20
3. A novelKITframe-shift mutation in a large Chinese family with variably severe phenotypes of piebaldism;The Journal of Dermatology;2012-10-22
4. Association of Piebaldism, Multiple Café-au-lait Macules, and Intertriginous Freckling: Clinical Evidence of a Common Pathway between KIT and Sprouty-Related, Ena/Vasodilator-Stimulated Phosphoprotein Homology-1 Domain Containing Protein 1 (SPRED1);Pediatric Dermatology;2012-09-28
5. Characterization of an alternative splicing by a NAGNAG splice acceptor site in the porcine KIT gene;Genes & Genomics;2011-04
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