K162E - A rare and uncategorized CFTR variant causing cystic fibrosis.

doi:10.1016/j.jcf.2020.07.007

Article

K162E - A rare and uncategorized CFTR variant causing cystic fibrosis.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society - 1 May 2021

Souza Edna Lúcia, Ribeiro Mota Laís, Leite Ferreira de Lima Renata Lúcia, Horejs Bittencourt Paloma, Castro Ribeiro Guedes Virgínia Maria, Salinas Danieli

Abstract excerpt

No abstract is available from the source.

Topics

Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Genetic Variation
Humans
Infant
Male

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.