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Number of items: 2.
2018
Khan, A. O., Budde, B. S., Nuernberg, P., Kawalia, A., Lenzner, S. and Bolz, H. J. (2018). Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotype. Clin. Genet., 93 (1). S. 149 - 155. HOBOKEN: WILEY. ISSN 1399-0004
2016
Khan, A. O., Tamimi, M., Lenzner, S. and Bolz, H. J. (2016). Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian Peninsula. Clin. Genet., 90 (1). S. 96 - 99. HOBOKEN: WILEY-BLACKWELL. ISSN 1399-0004