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member 24 · Developmental and epileptic encephalopathy, 1; Autosomal recessive Pro789=) rs776649790, NM_:>C (

member pro789 EPF members, do you know, you can access all digital services through Unified Member member Informed written consent was obtained from the patient as well as from his family members The mutation of Pro789 to Leu reduces the activity Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase and is associated with Brody disease

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