Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy
- PMID: 4543600
- DOI: 10.1111/j.1399-0004.1973.tb01140.x
Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy
Similar articles
-
[General amyloidosis with lattice dystrophy of the cornea].Duodecim. 1971;87(21):1412-9. Duodecim. 1971. PMID: 5315643 Finnish. No abstract available.
-
Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome.Ann Clin Res. 1969 Dec;1(4):314-24. Ann Clin Res. 1969. PMID: 4313418 No abstract available.
-
Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.J Neurol Neurosurg Psychiatry. 1979 Nov;42(11):1020-30. doi: 10.1136/jnnp.42.11.1020. J Neurol Neurosurg Psychiatry. 1979. PMID: 228009 Free PMC article.
-
[Hereditary gelsolin amyloidosis--40 years of Meretoja disease].Duodecim. 2010;126(10):1162-71. Duodecim. 2010. PMID: 20597346 Review. Finnish.
-
Hereditary gelsolin amyloidosis.Handb Clin Neurol. 2013;115:659-81. doi: 10.1016/B978-0-444-52902-2.00039-4. Handb Clin Neurol. 2013. PMID: 23931809 Review.
Cited by
-
Mutation in gelsolin gene in Finnish hereditary amyloidosis.J Exp Med. 1990 Dec 1;172(6):1865-7. doi: 10.1084/jem.172.6.1865. J Exp Med. 1990. PMID: 2175344 Free PMC article.
-
The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene.Ann Lab Med. 2016 May;36(3):259-62. doi: 10.3343/alm.2016.36.3.259. Ann Lab Med. 2016. PMID: 26915616 Free PMC article.
-
The Finnish Disease Heritage III: the individual diseases.Hum Genet. 2003 May;112(5-6):470-526. doi: 10.1007/s00439-002-0877-1. Epub 2003 Mar 8. Hum Genet. 2003. PMID: 12627297 Review.
-
Genetics in an isolated population like Finland: a different basis for genomic medicine?J Community Genet. 2017 Oct;8(4):319-326. doi: 10.1007/s12687-017-0318-4. Epub 2017 Jul 20. J Community Genet. 2017. PMID: 28730583 Free PMC article.
-
A DNA test for Indiana/Swiss hereditary amyloidosis (FAP II).Am J Hum Genet. 1988 Aug;43(2):182-7. Am J Hum Genet. 1988. PMID: 2840822 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources