Cite
HARVARD Citation
Intarak, N. et al. (2018). Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia. British journal of dermatology. pp. 758-760. [Online].
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Intarak, N. et al. (2018). Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia. British journal of dermatology. pp. 758-760. [Online].