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- Title
Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1–4 genes and practical aspects.
- Authors
Rooryck, Caroline; Morice-Picard, Fanny; Elçioglu, Nursel H.; Lacombe, Didier; Taieb, Alain; Arveiler, Benoît
- Abstract
A letter to the editor is presented about oculocutaneous albinism (OCA), an autosomal recessive disease of the skin, hair and eye hypopigmentation caused by melanin biosynthesis deficiency.
- Subjects
LETTERS to the editor; ALBINOS &; albinism
- Publication
Pigment Cell & Melanoma Research, 2008, Vol 21, Issue 5, p583
- ISSN
1755-1471
- Publication type
Letter
- DOI
10.1111/j.1755-148X.2008.00496.x