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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family
A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family
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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

Callea, M ; Nieminen, P ; Willoughby, C E ; Clarich, G ; Yavuz, I ; Vinciguerra, A ; Di Stazio, M ; Giglio, S ; Sani, I ; Maglione, M ; Pensiero, S ; Tadini, G ; Bellacchio, E

Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Vol.30 (2), p.341-343

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  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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