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Gahl, W.A., Brantly, M., Kaiser-Kupfer, M.I., Iwata, F., Hazelwood, S., Shotelersuk, V., Duffy, L.F., Kuehl, E.M., Troendle, J. and Bernardini, I. (1998) Genetic Defects and Clinical Characteristics of Patients with a Form of Oculocutaneous Albinism (Hermansky-Pudlak Syndrome). The New England Journal of Medicine, 338, 1258-1264.
http://dx.doi.org/10.1056/NEJM199804303381803
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