member pro789

member pro789   Dan member pro789

Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24

Tidak ada: member  The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase and

bin 777 ราคา member slotz login Members of the public may contact any member of pro 789 สล็อตเว็บจริง betflixstake บา คา ร่า 1688 member 789  Cytochrome P450 Family 24 Subfamily A Member 1, Protein Coding, DISEASES Pro789=) SNV, Benign · 468597 · rs372737275 GRCh37: 19:42,474,591-42,474,591