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Two novel mutations in exon 3 of PHOX2B gene: think about congenital central hypoventilation syndrome in patients with Hirschsprung disease

Crossref DOI link: https://doi.org/10.1186/s13052-019-0636-8

Published Online: 2019-04-18

Published Print: 2019-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Paglietti, Maria Giovanna

Cherchi, Claudio https://orcid.org/0000-0003-1628-5488
Porcaro, Federica

Agolini, Emanuele

Schiavino, Alessandra

Petreschi, Francesca

Novelli, Antonio

Cutrera, Renato
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Text and Data Mining valid from 2019-04-18
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Article History

Received: 19 September 2018

Accepted: 29 March 2019

First Online: 18 April 2019

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