Article Versions Notes

Masson E, Wangermez M, Tougeron D, Rebours V, Férec C, Chen J-M. Compound Heterozygous Complete Loss-of-Function SPINK1 Variants as a Novel Cause of Severe Infantile Isolated Exocrine Pancreatic Insufficiency. Genes. 2025; 16(9):998. https://doi.org/10.3390/genes16090998

Masson, Emmanuelle, Marc Wangermez, David Tougeron, Vinciane Rebours, Claude Férec, and Jian-Min Chen. 2025. "Compound Heterozygous Complete Loss-of-Function SPINK1 Variants as a Novel Cause of Severe Infantile Isolated Exocrine Pancreatic Insufficiency" Genes 16, no. 9: 998. https://doi.org/10.3390/genes16090998

Masson, E., Wangermez, M., Tougeron, D., Rebours, V., Férec, C., & Chen, J.-M. (2025). Compound Heterozygous Complete Loss-of-Function SPINK1 Variants as a Novel Cause of Severe Infantile Isolated Exocrine Pancreatic Insufficiency. Genes, 16(9), 998. https://doi.org/10.3390/genes16090998