论文信息 - Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene. - 字舞流文

Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene.

A. Poulos | J. Weber | M. Schröder | R. Hurwitz | A. Klein | K. Harzer | D. Schnabel | B. Paton | W. Fürst | T. Zenk | Konrad Sandhoff | Kunihiko Suzuki | Doris SchnabelS | Maria Schroderl | Werner Furst | Andreas Klein | Robert HurwitzS | Thomas Zenk | Jurgen Weberg | Klaus HarzerT | Barbara C. Patonil | Alf Poulos