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المؤلفون: Torunn Fiskerstrand, Helge Boman, Jaran Apold, Khanh Pham, Siv L Tonder, Najla Arshad, Stefan Johansson, Rune Rose Tronstad, Sandhya S. Visweswariah, Nils Hovdenak, Bjørn Ivar Haukanes, Bjarte Håvik, Damien Brackman, Kabir H. Biswas, Shawn Levy, Per M. Knappskog
المصدر: New England Journal of Medicine. 366:1586-1595
مصطلحات موضوعية: Diarrhea, Male, Heterozygote, medicine.medical_specialty, Receptors, Peptide, Genetic Linkage, Mutation, Missense, Receptors, Enterotoxin, medicine.disease_cause, Polymorphism, Single Nucleotide, Inflammatory bowel disease, Cystic fibrosis, Proinflammatory cytokine, Internal medicine, medicine, Humans, Missense mutation, Cyclic GMP, Exome sequencing, Mutation, business.industry, Heterozygote advantage, General Medicine, medicine.disease, Pedigree, Endocrinology, Receptors, Guanylate Cyclase-Coupled, Chronic Disease, Female, medicine.symptom, business, Signal Transduction