Investigation of the ABC transporter MRP1 in selected patients with presumed defects in vitamin B12 absorption.
about
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicitiesInherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.Hereditary intrinsic factor deficiency in chaldeans.An exon 53 frameshift mutation in CUBN abrogates cubam function and causes Imerslund-Gräsbeck syndrome in dogsABCC1 transports cytosolic Cbl to extracellular region
P2860
Investigation of the ABC transporter MRP1 in selected patients with presumed defects in vitamin B12 absorption.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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name
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
@en
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
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type
label
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
@en
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
@nl
prefLabel
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
@en
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
@nl
P2093
P1433
P1476
Investigation of the ABC trans ...... cts in vitamin B12 absorption.
@en
P2093
Amy C Sturm
Cameron M Beech
Nidhi P Shah
Stephan M Tanner
P304
P356
10.1182/BLOOD-2010-12-322750
P407
P577
2011-04-01T00:00:00Z