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Functional impairment of lens aquaporin in two families with dominantly inherited cataracts
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
11001937
retrieved
26 November 2016
title
Functional impairment of lens aquaporin in two families with dominantly inherited cataracts
(English)
1 reference
stated in
PubMed
PubMed ID
11001937
retrieved
26 November 2016
author name string
V Berry
series ordinal
4
0 references
S S Bhattacharya
series ordinal
8
0 references
P Francis
series ordinal
1
0 references
P Agre
series ordinal
9
0 references
M Yasui
series ordinal
3
0 references
M K Wyatt
series ordinal
6
0 references
J J Chung
series ordinal
2
0 references
G Wistow
series ordinal
7
0 references
A Moore
series ordinal
5
0 references
language of work or name
English
0 references
publication date
22 September 2000
0 references
published in
Human Molecular Genetics
1 reference
stated in
PubMed
volume
9
0 references
issue
15
0 references
page(s)
2329-34
0 references
cites work
Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels
1 reference
stated in
COCI
retrieved
11 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/citations/10.1126/SCIENCE.7521540
Identifiers
DOI
10.1093/OXFORDJOURNALS.HMG.A018925
0 references
PubMed ID
11001937
1 reference
stated in
PubMed
PubMed ID
11001937
retrieved
26 November 2016
ResearchGate publication ID
12321506
0 references
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