All individuals with variants in gene LONP1

19 entries on 1 page. Showing entries 1 - 19.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00032322 - PubMed: Strauss 2015, Journal: Strauss 2015, Shebib 1991 - - - Canada Mennonite, German - - - - CODAS see paper 1 1 Johan den Dunnen
00032323 - PubMed: Strauss 2015, Journal: Strauss 2015 - - - Canada European (mixed) - - - - CODAS see paper; .. 2 1 Johan den Dunnen
00032324 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00032325 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00032326 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00032327 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00032328 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00032329 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00032330 - PubMed: Strauss 2015, Journal: Strauss 2015 - - yes United States Amish, Swiss - - - - CODAS see paper; .. 1 1 Johan den Dunnen
00163815 - - - M yes Afghanistan - - - - - neurodegeneration - 1 1 Grace Yoon
00296613 Pat46 PubMed: Taylor 2014 - M - Germany - - - - - ? muscle affected; central nervous system not affected; heart not affected; liver not affected; progressive external ophthalmoparesis, lactic acidosis, raised CK (800) 2 1 Johan den Dunnen
00385500 16022871 PubMed: Lenassi 2020 retrospective analysis M - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00414415 WHP82 PubMed: Sun 2018 - F - China - - - - - ? - 2 1 LOVD
00441892 Fam24 PubMed: Khan 2015 2-generation family, 3 affected sibs (2F, M) - yes Saudi Arabia - - - - - CTRCT congenital cataract, nuclear 1 3 Johan den Dunnen
00444956 11DG1104 PubMed: Patel 2017 simplex case - - - - - - - - CTRCT pediatric nuclear cataract; not syndromic 1 1 Johan den Dunnen
00444967 13DG0017 PubMed: Patel 2017 family - - - - - - - - CTRCT congenital cataract; not syndromic 1 5 Johan den Dunnen
00444974 14DG0067 PubMed: Patel 2017 family - - - - - - - - CTRCT pediatric cataract; not syndromic 1 2 Johan den Dunnen
00444975 14DG0179 PubMed: Patel 2017 simplex case - - - - - - - - CTRCT congenital cataract as part of CODAS syndrome; syndromic 1 1 Johan den Dunnen
00444976 14DG0246 PubMed: Patel 2017 simplex case - - - - - - - - CTRCT congenital cataract; not syndromic 1 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.