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Edvardson S, Korman SH, Livne A, Shaag A, Saada A, Nalbandian R, Allouche-Arnon H, Gomori JM, Katz-Brull R (2010) l-arginine:glycine amidinotransferase (AGAT) deficiency: clinical presentation and response to treatment in two patients with a novel mutation

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Previously, we have established genetic statistics to detect genetic variation in complex diseases and used MR approaches to evaluate the causal relationships between complex diseases, including the casual association of Hcy with NAFLD (4654)