Recurrence of pulmonary alveolar proteinosis after bilateral lung transplantation in a patient with a nonsense mutation in CSF2RB

Abstract Hereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB , which encode GM-CSF receptor α and β respectively, is a rare disease. Although some experimental therapeutic strategies have been proposed, no clinical evidence has yet been reported. We herein describ...

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Veröffentlicht in:Respiratory medicine case reports 2016-01, Vol.19, p.89-93
Hauptverfasser: Takaki, Masahiro, Tanaka, Takeshi, Komohara, Yoshihiro, Tsuchihashi, Yoshiko, Mori, Daisuke, Hayashi, Kentaro, Fukuoka, Junya, Yamasaki, Naoya, Nagayasu, Takeshi, Ariyoshi, Koya, Morimoto, Konosuke, Nakata, Koh
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Sprache:eng
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