Jin Xu

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.

T. Gilliam, S. Zeitlin, C. Mekios, 1999, Human molecular genetics.

Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

G. Penchaszadeh, T. Carter, E. Vitale, 1995, American journal of human genetics.