
PAA848Hu01 | Homo sapiens (Human)
GPMM; Phosphorylase,Glycogen; McArdle Syndrome,Glycogen Storage Disease Type V; Myophosphorylase

MAA848Hu22 | Homo sapiens (Human)
GPMM; Phosphorylase,Glycogen; McArdle Syndrome,Glycogen Storage Disease Type V; Myophosphorylase
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