Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease - Concepedia

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Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

64

Citations

9

References

1992

Year

C. P. J. Maury, Juha Kere, Riina Tolvanen, Albert de la Chapelle

UrologyMedicineGeneticsRenal PathologyAsn187 Gelsolin MutationPathologyProtein MisfoldingSevere Renal DiseaseChronic Kidney DiseaseFinnish-type Familial AmyloidosisNephrology

References

	Year	Citations

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