Publications:

Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.

Human Genetics

Tollefson, Mallory R MR; Gogal, Rose A RA; Weaver, A Monique AM; Schaefer, Amanda M AM; Marini, Robert J RJ; Azaiez, Hela H; Kolbe, Diana L DL; Wang, Donghong D; Weaver, Amy E AE; Casavant, Thomas L TL; Braun, Terry A TA; Smith, Richard J H RJH; Schnieders, Michael J MJ

Publication Date: 2023-04-22

Variant appearance in text: COL4A5: 3419G>T; Gly1140Val

PubMed Link: 37086329

Variant Present in the following documents:

• 439_2023_2559_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

Trimerization and Genotype-Phenotype Correlation of COL4A5 Mutants in Alport Syndrome.

Kidney International Reports

Kamura, Misato M; Yamamura, Tomohiko T; Omachi, Kohei K; Suico, Mary Ann MA; Nozu, Kandai K; Kaseda, Shota S; Kuwazuru, Jun J; Shuto, Tsuyoshi T; Iijima, Kazumoto K; Kai, Hirofumi H

Publication Date: 2020-05

Variant appearance in text: COL4A5: G1140V

PubMed Link: 32405592

Variant Present in the following documents:

• Main text
• main.pdf
• mmc1.pdf

View BVdb publication page

Determination of cystathionine beta-synthase activity in human plasma by LC-MS/MS: potential use in diagnosis of CBS deficiency.

Journal Of Inherited Metabolic Disease

Krijt, Jakub J; Kopecká, Jana J; Hnízda, Aleš A; Moat, Stuart S; Kluijtmans, Leo A J LA; Mayne, Philip P; Kožich, Viktor V

Publication Date: 2011-02

Variant appearance in text: ATS: G1140V

PubMed Link: 20821054

Variant Present in the following documents:

• 10545_2011_Article_9371.pdf

View BVdb publication page