Childhood-onset inflammatory bowel diseases associated with mutation of Wiskott-Aldrich syndrome protein gene
Takashi Ohya(Tokyo Medical and Dental University), Shuichi Ito(Yokohama City University)
Cited by 21
Related Papers
Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy
|The American Journal of Human Genetics|2013|224
Tolerability and safety of a new elimination diet for pediatric eosinophilic gastritis and duodenitis
|Allergology International|2022|13