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3. 10.1038/ng0895-409 9) Kere J, Srivastava AK, et al : X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 13: 409-416, 1996. 

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4. 10.1038/11937 10) Monreal AW, Ferguson BM, et al : Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet 22: 366-369, 1999. 

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5. 10.1016/j.ajhg.2009.06.001 12) Bohring A, Stamm T, et al : WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. Am J Hum Genet 85: 97-105, 2009. 

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6. 10.1002/humu.21384 13) Cluzeau C, Hadj-Rabia S, et al : Only four genes ( EDA1 , EDAR , EDARADD ,and WNT10A ) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. Hum Mutat 32: 70-77, 2011. 

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7. 10.1093/hmg/8.11.2079 14) Ezer S, Bayés M, et al : Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells. Hum Mol Genet 8: 2079-2086, 1999. 

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8. 16) Winiewski SA, Kobielak A, et al : Recent advances in understanding of the molecular basis of anhidrotic ectodermal dysplasia: discovery of a ligand, ectodysplasin A and its two receptors. J Appl Genet 43: 97-107, 2002. 

9. 10.4161/cc.5.21.3403 17) Cui CY and Schlessinger D : EDA signaling and skin appendage development. Cell Cycle 5: 2477-2483, 2006. 

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10. 10.1002/ajmg.a.32855 18) Mikkola ML : Molecular aspects of hypohidrotic ectodermal dysplasia. Am J Med Genet A 149A: 2031- 2036, 2009. 

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11. 10.1073/pnas.131076098 19) Chen Y, Molloy SS, et al : Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia. Proc Natl Acad Sci U S A 98: 7218-7223, 2001. 

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12. 10.1007/s10038-006-0389-2 20) Tao R, Jin B, et al : A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia. J Hum Genet 51: 498-502, 2006. 

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13. 10.1002/ajmg.a.33840 21) Kantaputra P, Sripathomsawat W : WNT10A and isolated hypodontia. Am J Med Genet A 155A: 1119-1122, 2011. 

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14. 10.1002/ajmg.a.34045 22) Bergendal B, Klar J, et al : Isolated oligodontia associated with mutations in EDARADD , AXIN2 , MSX1 , and PAX9 genes. Am J Med Genet A 155A: 1616-1622, 2011. 

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