Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Dilytė, E."'
Publikováno v:
Acta Dermatovenerologica Croatica
Volume 28
Issue 3
Scopus-Elsevier
Issue 2
Volume 28
Issue 3
Scopus-Elsevier
Issue 2
T Piebaldism is a rare, autosomal dominant disorder characterized by the congenital absence of melanocytes in affected areas of the skin and hair. We report on a familial 4q12 deletion that involves the KIT gene and causes piebaldism in affected indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::08125f424d3ab454a0d9bde40879342e
https://hrcak.srce.hr/246868
https://hrcak.srce.hr/246868
