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    Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutation

    Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutation by Parodi, S, Vollono, C, Baglietto, MP, Balestri, M, Di Duca, M, Landri, PA, Ceccherini, I, Ottonello, G, Cilio, MR

    Published in Clinical genetics
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