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5 in total

1. Assignment of the gene for human sphingolipid activator protein-2 (SAP-2) to chromosome 10.

Authors: S Fujibayashi; F T Kao; C Jones; H Morse; M Law; D A Wenger
Journal: Am J Hum Genet Date: 1985-07 Impact factor: 11.025

2. Insertion in the mRNA of a metachromatic leukodystrophy patient with sphingolipid activator protein-1 deficiency.

Authors: X L Zhang; M A Rafi; G DeGala; D A Wenger
Journal: Proc Natl Acad Sci U S A Date: 1990-02 Impact factor: 11.205

3. Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological study.

Authors: W Schlote; K Harzer; H Christomanou; B C Paton; B Kustermann-Kuhn; B Schmid; J Seeger; U Beudt; I Schuster; U Langenbeck
Journal: Eur J Pediatr Date: 1991-06 Impact factor: 3.183

4. Correction of sulfatide metabolism after transfer of prosaposin cDNA to cultured cells from a patient with SAP-1 deficiency.

Authors: M A Rafi; S Amini; X L Zhang; D A Wenger
Journal: Am J Hum Genet Date: 1992-06 Impact factor: 11.025

5. The gene coding for a sphingolipid activator protein, SAP-1, is on human chromosome 10.

Authors: K Inui; F T Kao; S Fujibayashi; C Jones; H G Morse; M L Law; D A Wenger
Journal: Hum Genet Date: 1985 Impact factor: 4.132

5 in total