Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.

Maury CP, Kere J, Tolvanen R, de la Chapelle A

DOI: 10.1016/0014-5793(90)80510-p
Published: 1990 Dec 10
Container: FEBS letters
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1016/0014-5793-90-80510-p,
  title = {Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.},
  author = {Maury CP and Kere J and Tolvanen R and de la Chapelle A},
  year = {1990},
  journal = {FEBS letters},
  doi = {10.1016/0014-5793(90)80510-p},
  url = {https://doi.org/10.1016/0014-5793(90)80510-p}
}

RIS

TY  - JOUR
TI  - Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.
AU  - Maury CP
AU  - Kere J
AU  - Tolvanen R
AU  - de la Chapelle A
PY  - 1990
JO  - FEBS letters
DO  - 10.1016/0014-5793(90)80510-p
UR  - https://doi.org/10.1016/0014-5793(90)80510-p
ER  -

APA

CP, M., J, K., R, T., & A, D. L. C. (1990). Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.. FEBS letters. https://doi.org/10.1016/0014-5793(90)80510-p

Source records

pubmed · retrieved 2026-11-11T01:15:14.882Z