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									<identifier>oai:www.peertechzpublications.org:10.17352/acn.000044</identifier>
									<datestamp>2020-11-27</datestamp>
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										Arterial hypertension in children with Williams-Beuren syndrome
										</dc:title><dc:creator>Novo Marta</dc:creator><dc:creator> Loureiro Marília</dc:creator><dc:creator>Rocha Liliana</dc:creator><dc:description>&lt;p&gt;Williams-Beuren Syndrome (WBS) is a multisystemic disorder with prevalence of 1/7500 [1], affects both genders equally and it is caused by a microdeletion of 26-28 genes, including elastin and NCF1 genes, of the chromosome region 7q11.23 [1,2]. The disease is transmitted in an autosomal dominant fashion, but almost all cases are the result of de novo mutations [1].&amp;nbsp;&lt;/p&gt;</dc:description>
										<dc:publisher>Archives of Clinical Nephrology - Peertechz Publications</dc:publisher>
										<dc:date>2020-11-27</dc:date>
										<dc:type>Short Communication</dc:type>
										<dc:identifier>https://doi.org/10.17352/acn.000044</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Novo Marta et al.</dc:rights>
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