Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability is a paper indexed in PICO Portal from OpenAlex.
How many citations does Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability have?
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability has 255 citations in the OpenAlex counts PICO Portal stores.
When was Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability published?
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability has 2000 year in the PICO Portal index.
What is the open-access status of Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability?
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability has green oa status in the PICO Portal index.
What is the DOI of Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability?
The DOI for Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability is on the source record.
What is the PMID of Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability?
The PMID for Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability is on the source record.
What is the OpenAlex record for Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability?
The OpenAlex for Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability is on the source record.