Cite
HARVARD Citation
Farooq, M. et al. (n.d.). A Homozygous Frameshift Mutation in the HOXC13 Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family. Human mutation. 34 (4), pp. 578-581. [Online].
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Farooq, M. et al. (n.d.). A Homozygous Frameshift Mutation in the HOXC13 Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family. Human mutation. 34 (4), pp. 578-581. [Online].