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Journal of Computer-Aided Molecular Design 17 , 643664 (2003)

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:) References Posey, D., & Mozayani, A

The most frequent genetic causes of SLOCA are heterozygous GAA expansions in FGF14 (spinocerebellar atrophy type 27B) and biallelic expansions in RFC1 (cerebellar ataxia with neuropathy and vestibular areflexia (CANVAS))

The presence of human CD31 (human-specific antibody) vascular structures that appear to have anastomosed into the mouse kidney parenchyma further supports the presence of vascularization within our organoids and ongoing de novo vascularization

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