Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.
about
Ion channels in renal disease.Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene.ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations.
P2860
Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.
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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2011年学术文章
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2011年学术文章
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2011年學術文章
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name
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@en
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@nl
type
label
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@en
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@nl
prefLabel
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@en
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@nl
P2093
P2860
P1476
Bartter syndrome in two sister ...... LCNKB gene, one with deafness.
@en
P2093
Aicha Merouani
Pierre Robitaille
P2860
P2888
P304
P356
10.1007/S00431-011-1464-Z
P577
2011-04-09T00:00:00Z