PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome (Q42718575)

From Wikidata
Jump to navigation Jump to search
scientific article published on May 2004
edit
Language Label Description Also known as
English
PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome
scientific article published on May 2004

    Statements

    PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome (English)
    1 reference
    I Matera
    1 reference
    T Bachetti
    1 reference
    F Puppo
    1 reference
    M Di Duca
    1 reference
    F Morandi
    1 reference
    G M Casiraghi
    1 reference
    M R Cilio
    1 reference
    R Hennekam
    1 reference
    R Hofstra
    1 reference
    J G Schöber
    1 reference
    R Ravazzolo
    1 reference
    G Ottonello
    1 reference
    I Ceccherini
    1 reference
    1 May 2004
    1 reference
    41
    1 reference
    373-380
    1 reference

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit