| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/ANA.410360418 |
| P8608 | Fatcat ID | release_uunnk2c25bftpdekcj7qg5wh3a |
| P698 | PubMed publication ID | 7944300 |
| P2093 | author name string | DiMauro S | |
| Haller RG | |||
| Shanske S | |||
| Brownell AK | |||
| Tsujino S | |||
| P2860 | cites work | Genomic organization of human lactate dehydrogenase-A gene | Q24529918 |
| Molecular characterization of gene expression in human lactate dehydrogenase-A deficiency | Q34350990 | ||
| Three new mutations in patients with myophosphorylase deficiency (McArdle disease) | Q35888850 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 661-665 | |
| P577 | publication date | 1994-10-01 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients | |
| P478 | volume | 36 |
| Q35624916 | Diagnostic evaluation of rhabdomyolysis |
| Q37609488 | Genomics and genetics in the biology of adaptation to exercise |
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| Q53062399 | Hereditary lactate dehydrogenase M-subunit deficiency with late-developing pustular psoriasis-like lesions. |
| Q35122361 | Inhibition of lactate dehydrogenase activity as an approach to cancer therapy |
| Q104617773 | Knockdown of lactate dehydrogenase by adeno-associated virus-delivered CRISPR/Cas9 system alleviates primary hyperoxaluria type 1 |
| Q38576245 | Metabolic Myoglobinuria |
| Q71408492 | Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindred |
| Q34299998 | Muscle glycogenoses |
| Q35076658 | Muscular cramps: proposals for a new classification |
| Q44037962 | Pregnancy complicated with lactate dehydrogenase M-subunit deficiency: the first case report |
| Q64044875 | Specific Inhibition of Hepatic Lactate Dehydrogenase Reduces Oxalate Production in Mouse Models of Primary Hyperoxaluria |
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