Glycinuria, a hereditary disorder associated with nephrolithiasis.
about
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transportersRenal tubular transport of proline, hydroxyproline, and glycine. 3. Genetic basis for more than one mode of transport in human kidney.RENAL TUBULAR TRANSPORT OF PROLINE, HYDROXYPROLINE, AND GLYCINE IN HEALTH AND IN FAMILIAL HYPERPROLINEMIA.Lessons from inborn errors of metabolism.The prognosis and management of renal tubular disordersHYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT.Diseases of JewsMaleic acid-induced inhibition of amino acid transport in rat kidney.Bibliography of Human Genetics*.
P2860
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P2860
Glycinuria, a hereditary disorder associated with nephrolithiasis.
description
1957 nî lūn-bûn
@nan
1957 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1957 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1957年の論文
@ja
1957年論文
@yue
1957年論文
@zh-hant
1957年論文
@zh-hk
1957年論文
@zh-mo
1957年論文
@zh-tw
1957年论文
@wuu
name
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@ast
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@en
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@nl
type
label
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@ast
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@en
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@nl
prefLabel
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@ast
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@en
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@nl
P2093
P1476
Glycinuria, a hereditary disorder associated with nephrolithiasis.
@en
P2093
P304
P356
10.1016/0002-9343(57)90320-0
P407
P577
1957-09-01T00:00:00Z