Pub. Date : 2007 Jul
PMID : 17915571
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | McArdle disease or Glycogenosis type V is an autosomal recessive metabolic disorder caused by a deficiency of the muscle isoform of glycogen phosphorylase (myophosphorylase, PYGM), the specific skeletal muscle enzyme that initiates glycogen breakdown. | Glycogen | glycogen phosphorylase, muscle associated | Homo sapiens |
| 2 | McArdle disease or Glycogenosis type V is an autosomal recessive metabolic disorder caused by a deficiency of the muscle isoform of glycogen phosphorylase (myophosphorylase, PYGM), the specific skeletal muscle enzyme that initiates glycogen breakdown. | Glycogen | glycogen phosphorylase, muscle associated | Homo sapiens |