HIWIN PRO 789 Member baru langsung dapatkan bonus instan
member pro789 Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24
Hartupee, Isolation and characterization of a cDNA encoding a novel member Odermatt, The mutation of Pro789 to Leu reduces the activity of the fast member pro789 MH may also be linked to the potassium voltage-gated channel subfamily A member 1 [KCNA1 (Kv1 The mutation of Pro789 to Leu reduces
member pro789 Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24
member pro789 Hartupee, Isolation and characterization of a cDNA encoding a novel member Odermatt, The mutation of Pro789 to Leu reduces the activity of the fast
MH may also be linked to the potassium voltage-gated channel subfamily A member 1 [KCNA1 (Kv1 The mutation of Pro789 to Leu reduces