Xun-ling Zhang

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

Mohammad A. Rafi, Gregory de Gala, Xun-ling Zhang et al. · Somatic Cell and Molecular Genetics · 1993 · 85 citations

Life Sciences, Genetics, Molecular Genetics +14

Detection of a point mutation in sphingolipid activator protein-1 mRNA in patients with a variant form of metachromatic leukodystrophy

Mohammad A. Rafi, Xun-ling Zhang, Gregory D. DeGala et al. · Biochemical and Biophysical Research Communications · 1990 · 62 citations

Life Sciences, Genetics, Molecular Genetics +16

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

Xun-ling Zhang, Mohammad A. Rafi, Gregory de Gala et al. · Human Genetics · 1991 · 43 citations

Life Sciences, Genetics, Molecular Biology +12

Regional localization of the gene coding for sphingolipid activator protein SAP-1 on human chromosome 10

Fa‐Ten Kao, M L Law, Judith A. Hartz et al. · Somatic Cell and Molecular Genetics · 1987 · 18 citations

Life Sciences, Genetics, Molecular Biology +8