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A new type of syndromic albinism associated with mutations in AP 3D1
Author(s) -
Montoliu Lluis,
Marks Michael S.
Publication year - 2017
Publication title -
pigment cell and melanoma research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.618
H-Index - 105
eISSN - 1755-148X
pISSN - 1755-1471
DOI - 10.1111/pcmr.12543
Subject(s) - albinism , decussation , melanosome , oculocutaneous albinism , biology , hypopigmentation , hermansky–pudlak syndrome , genetics , medicine , anatomy , pathology , melanin , pulmonary fibrosis , fibrosis
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