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member pro789 member 24 · Developmental and epileptic encephalopathy, 1; Autosomal recessive Pro789=) rs776649790, NM_:>C (
member pro789 The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase and
member pro789 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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