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APA Citation
Painsi, C., Aubell, K., Wolf, P., Hügel, R., & Lange‐Asschenfeldt, B. (2017). a case of Schöpf‐Schulz‐Passarge syndrome caused by c.1135C>T WNT10A missense mutation. Journal der Deutschen Dermatologischen Gesellschaft, 15, 455–457. http://access.bl.uk/ark:/81055/vdc_100044869804.0x000025