Cite
HARVARD Citation
Painsi, C. et al. (2017). A case of Schöpf‐Schulz‐Passarge syndrome caused by c.1135C>T WNT10A missense mutation. Journal der Deutschen Dermatologischen Gesellschaft. pp. 455-457. [Online].
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Painsi, C. et al. (2017). A case of Schöpf‐Schulz‐Passarge syndrome caused by c.1135C>T WNT10A missense mutation. Journal der Deutschen Dermatologischen Gesellschaft. pp. 455-457. [Online].