Homozygous mutation in ABCA3 Lipid-Transporter defect (EXON 9) and low level of surfactant protein C

Poeschl, J. and Ruef, P. and Griese, M. and Lohse, P. and Aslanidis, C. and Rahman, S. and Kichi, M. and Al Baridi, A. and Pappapil, H. and Koch, L. (2010) Homozygous mutation in ABCA3 Lipid-Transporter defect (EXON 9) and low level of surfactant protein C. KLINISCHE PADIATRIE, 222 (S01). S41. ISSN 0300-8630

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Item Type: Article
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin
Depositing User: Petra Gürster
Date Deposited: 16 Apr 2020 05:37
Last Modified: 16 Apr 2020 05:37
URI: https://pred.uni-regensburg.de/id/eprint/24647

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