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Journal Article
Busch, Jutta, Frank, Valeska, Bachmann, Nadine, Otsuka, Atoshi, Oji, Vinzenz 
ORCID: 0000-0003-1380-4828, Metze, Dieter, Shah, Krati, Danda, Sumita, Watzer, Bernhard, Traupe, Heiko, Bolz, Hanno J., Kabashima, Kenji ORCID: 0000-0002-0773-0554 and Bergmann, Carsten
(2012).
Mutations in the Prostaglandin Transporter SLCO2A1 Cause Primary Hypertrophic Osteoarthropathy with Digital Clubbing.
J. Invest. Dermatol., 132 (10).
S. 2473 - 2477.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 0022-202X
Khan, Arif O., Decker, Eva, Bachmann, Nadine, Bolz, Hanno J. and Bergmann, Carsten (2016). C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophies. Ophthalmic Genet., 37 (3). S. 290 - 294. PHILADELPHIA: TAYLOR & FRANCIS INC. ISSN 1744-5094