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Results: 1 to 9 of 9
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hyperkalemic Periodic Paralysis Type 1 Molecular Genetics Laboratory London Health Sciences Centre Canada | 3 | 1 |
|
Muscle Channelopathy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 4 | 5 |
|
Hypokalemic periodic paralysis Genetic Analysis (CACNA1S 4 Mutations & SCN4A 5 Mutation) Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 1 |
|
Hypokalemic Periodic Paralysis: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 3 |
|
CeGaT GmbH Germany | 4 | 5 |
|
Bartter Syndrome incl. differential diagnosis Panel CeGaT GmbH Germany | 10 | 6 |
|
Hypokalemic periodic paralysis, CACNA1S sequencing Molecular Diagnostics Laboratory Seoul National University Hospital South Korea | 1 | 1 |
|
Familial Hypokalemic periodic paralysis, SCN4A sequencing Molecular Diagnostics Laboratory Seoul National University Hospital South Korea | 1 | 1 |
|
Hypokaleimc Periodic Paralysis Molecular Genetics Laboratory BC Children's and BC Women's Hospitals Canada | 1 | 2 |
|
Results: 1 to 9 of 9
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