G. Gala

发表

Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiency

D. Wenger, Xunxiao Zhang, M. Rafi, 1993, Somatic cell and molecular genetics.

The mechanism for a 33-nucleotide insertion in mRNA causing sphingolipid activator protein (SAP-1)-deficient metachromatic leukodystrophy

D. Wenger, Xunxiao Zhang, M. Rafi, 1991, Human Genetics.

Metachromatic leukodystrophy among southern Alaskan Eskimos: molecular and genetic studies

N. Pastor-Soler, D. Wenger, M. Rafi, 1995, Journal of Inherited Metabolic Disease.

Cloning and expression of cDNA encoding human galactocerebrosidase, the enzyme deficient in globoid cell leukodystrophy.

D. Wenger, M. Rafi, G. Gala, 1993, Human molecular genetics.