Entries of Al baridi, A on the publication server
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2010
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).
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