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Publications by Fadi Haddad
Molecular Basis of Oculocutaneous Albinism Type 1 in Lebanese Patients
Journal of Human Genetics
Genetics
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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
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan
American Journal of Human Genetics
Genetics
Oculocutaneous Albinism Among Schoolchildren in Harare, Zimbabwe.
Journal of Medical Genetics
Genetics
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
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Genetic Studies of TYRP1 and SLC45A2 in Pakistani Patients With Nonsyndromic Oculocutaneous Albinism
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology