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A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia

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Acknowledgements

We are indebted to all individuals who have participated in, or helped with, for our research. This study was supported by the National Natural Science Foundation of China (nos. 31371298, 81301151 and 81272023); Program for New Century Excellent Talents in University (NCET-13-0452); Wu Jieping Medical Foundation (no. 320.6750.13307); Youth Innovation Foundation of the First Affiliated Hospital of Xi’an Jiaotong University (no. 2013YK23); the National Innovation Experiment Programme for University Students (no. 201310698075); the Key Project of International Scientific Cooperation of Shaanxi Province (no. S2013KW25-02); and the Fundamental Research Funds for the Central Universities (no. 2012JDGZ07 and XJJ2012124).

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Correspondence to RUI ZHANG or JIE MA.

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[Li D., Xu R., Huang F., Wang B., Tao Y., Jiang Z., Li H., Yao J., Xu P., Wu X., Ren L., Zhang R., Kelsoe J. R. and Ma J. 2015 A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia. J. Genet. 94, xx–xx]

Daxu Li, Ran Xu and Fumeng Huang contributed equally to this work.

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LI, D., XU, R., HUANG, F. et al. A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia. J Genet 94, 115–119 (2015). https://doi.org/10.1007/s12041-015-0474-4

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