M., G., J.S., W., A., H., M., W., R., W., L.V., W., . . . SCHOOL, D. M. (2019). Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome).
استشهاد بنمط شيكاغوM., Glover, et al. Detection of Mutations in KLHL3 and CUL3 in Families With Fhht (familial Hyperkalaemic Hypertension or Gordon's Syndrome). 2019.
MLA استشهادM., Glover, et al. Detection of Mutations in KLHL3 and CUL3 in Families With Fhht (familial Hyperkalaemic Hypertension or Gordon's Syndrome). 2019.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.