about
HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice.Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects.Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome.High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies.TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss.Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women.Factors predicting vitamin D response variation in non-Hispanic white postmenopausal womenAssociation analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.[Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus].[Mapping of pathogenic genes in two families with autosomal dominant ichthyosis vulgaris]Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndrome
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-4882-4856
@en
name
Fengxiao Bu
@ast
Fengxiao Bu
@en
Fengxiao Bu
@nl
type
label
Fengxiao Bu
@ast
Fengxiao Bu
@en
Fengxiao Bu
@nl
prefLabel
Fengxiao Bu
@ast
Fengxiao Bu
@en
Fengxiao Bu
@nl
P106
P31
P496
0000-0002-4882-4856