-
Iminoglycinuria is an
autosomal recessive disorder of
renal tubular transport affecting reabsorption of the
amino acid glycine, and the
imino acids proline...
- PMID 8976113.
Rosenberg LE,
Durant JL,
Elsas LJ (June 1968). "Familial
iminoglycinuria. An
inborn error of
renal tubular transport". The New
England Journal...
-
Illyngophobia Ilyina–Amoashy–Grygory
syndrome Imaizumi–Kuroki
syndrome Iminoglycinuria Immotile cilia syndrome, due to
defective radial spokes Immotile cilia...
-
transcript variants.
Mutation in the SLC6A20 gene are ****ociated with
iminoglycinuria. One of a
cluster of 6
genes (SLC6A20, LZTFL1, CCR9, FYCO1, CXCR6 and...
- gamma-aminobutyric acid.
Mutations in the SLC36A2 gene are ****ociated with
Iminoglycinuria.
Proton coupled amino acid
transporter GRCh38:
Ensembl release 89:...
-
transporters are
located throughout this tissue. In
hereditary disease iminoglycinuria,
there is a
defect in the
human proton-coupled
amino acid transporter...
- for
sodium ions.
Mutations in the SLC6A18 gene are ****ociated with
iminoglycinuria. GRCh38:
Ensembl release 89: ENSG00000164363 – Ensembl, May 2017 GRCm38:...
- reabsorption.[citation needed]
Examples of
these disorders include Iminoglycinuria,
renal tubular acidosis and
Gitelman syndrome.[citation needed] v t...
- Auray-Blais, C; Cavanaugh, JA; Bröer, A; Rasko, JE (December 2008). "
Iminoglycinuria and
hyperglycinuria are
discrete human phenotypes resulting from complex...
- Ichthyosis, X-linked; 308100; STS
Iminoglycinuria, digenic; 242600; SLC36A2
Iminoglycinuria, digenic; 242600; SLC6A19
Iminoglycinuria, digenic; 242600; SLC6A20...
