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Oe Y, Mishima E, Mori T, Okamoto K, et al. A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis
with Alport Syndrome-like Phenotype. Intern Med 2021;60:2991-2996.
PMID: 33814499
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Oe Y, Mishima E, Mori T, Okamoto K, et al. A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis
with Alport Syndrome-like Phenotype. Intern Med 2021;60:2991-2996.
PMID: 33814499
|
|
|
|