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Publications by Richard A. SPRITZ

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

Biochemical Journal
BiochemistryCell BiologyMolecular Biology
2001English

Related publications

Molecular Basis of Oculocutaneous Albinism Type 1 in Lebanese Patients

Journal of Human Genetics
Genetics
2005English

Oculocutaneous Albinism Type 1

2020English

Minimal Pigment Oculocutaneous Albinism Type 1

2020English

Oculocutaneous Albinism Type 1A

2020English

Oculocutaneous Albinism Type 6

2020English

Temperature-Sensitive Tyrosinase Associated With Peripheral Pigmentation in Oculocutaneous Albinism.

Journal of Clinical Investigation
Medicine
1991English

Biology and Genetics of Oculocutaneous Albinism and Vitiligo – Common Pigmentation Disorders in Southern Africa

South African Medical Journal
Medicine
2013English

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

American Journal of Human Genetics
Genetics
2004English

Oculocutaneous Albinism and West Syndrome- A Rare Association

Journal of Evolution of Medical and Dental Sciences
2019English

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