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Publications by Hala Zahreddine

Molecular Basis of Oculocutaneous Albinism Type 1 in Lebanese Patients

Journal of Human Genetics

English

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The Molecular Basis of Oculocutaneous Albinism Type 1 (OCA1): Sorting Failure and Degradation of Mutant Tyrosinases Results in a Lack of Pigmentation

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Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan

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Oculocutaneous Albinism Among Schoolchildren in Harare, Zimbabwe.

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Mild Form of Oculocutaneous Albinism Type 1: Phenotypic Analysis of Compound Heterozygous Patients With the R402Q Variant of the TYR Gene

British Journal of Ophthalmology

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Genetic Studies of TYRP1 and SLC45A2 in Pakistani Patients With Nonsyndromic Oculocutaneous Albinism

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