Homozygous mutation in ABCA3 Lipid-Transporter defect (EXON 9) and low level of surfactant protein C
Pöschl, J, Ruef, P, Griese, M, Lohse, P, Aslanidis, C, Rahman, S, Kichi, M, Al baridi, A, Pappapil, H and Koch, L (2010) Homozygous mutation in ABCA3 Lipid-Transporter defect (EXON 9) and low level of surfactant protein C. Klinische Pädiatrie 222 (S 01).Date of publication of this fulltext: 19 Dec 2024 11:36
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| Item type | Article | ||||
| Journal or Publication Title | Klinische Pädiatrie | ||||
| Publisher: | GEORG THIEME VERLAG KG | ||||
|---|---|---|---|---|---|
| Place of Publication: | STUTTGART | ||||
| Volume: | 222 | ||||
| Number of Issue or Book Chapter: | S 01 | ||||
| Date | 2010 | ||||
| Institutions | Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin | ||||
| Identification Number |
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| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 66085 |
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