Association of ion transporters with CLD.

Association of ion transporters with CLD.

<div><p>Objective</p><p>The autosomal recessive disease congenital chloride diarrhea (CLD), caused by loss-of-function mutations in the <i>solute carrier family 26 member 3</i> (<i>SLC26A3</i>) gene, shows association with inflammatory bowel disease (I...

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Bibliographic Details
Main Author: Satu Wedenoja (12850876) (author)
Other Authors: Jarmo Ritari (176127) (author), Jukka Partanen (89192) (author), Juha Kere (11900) (author), Kaija-Leena Kolho (6168578) (author)
Published: 2025
Subjects:
Biochemistry
Genetics
Physiology
Infectious Diseases
Virology
Chemical Sciences not elsewhere classified
inflammatory bowel disease
congenital chloride diarrhea
finnish founder mutation
data demonstrate enrichment
cld ), caused
finnish patients
xlink ">
slc26a3 interacts
slc26a3 </
shows association
p </
intestinal inflammation
immune signatures
ibd ).
function mutations
chromosomes harboring
>) gene
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