Cite
HARVARD Citation
Ralser, D. et al. (2020). Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome. British journal of dermatology. pp. 756-757. [Online].
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Ralser, D. et al. (2020). Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome. British journal of dermatology. pp. 756-757. [Online].