about
Deep dermatophytosis and inherited CARD9 deficiencyEvaluation of approaches to identify associated SNPs that explain the linkage evidence in nuclear families with affected siblingsPartial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds.Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation.Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients.Clinical epidemiology of laboratory-confirmed Buruli ulcer in Benin: a cohort study.Findings in patients from Benin with osteomyelitis and polymerase chain reaction-confirmed Mycobacterium ulcerans infection.Quantifying genomic imprinting in the presence of linkage.HIV infection and Buruli ulcer in Africa.Lemierre syndrome with meningo-encephalitis, severe cerebral artery stenosis, and focal neurological symptoms.Defining and targeting high-risk populations in Buruli ulcer–Authors' reply
P50
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P50
description
Forscher
@de
chercheur
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investigador
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onderzoeker
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researcher
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հետազոտող
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研究者
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name
Quentin B Vincent
@ast
Quentin B Vincent
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Quentin B Vincent
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Quentin B Vincent
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type
label
Quentin B Vincent
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Quentin B Vincent
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Quentin B Vincent
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Quentin B Vincent
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prefLabel
Quentin B Vincent
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Quentin B Vincent
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Quentin B Vincent
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Quentin B Vincent
@nl
P106
P21
P31
P496
0000-0001-6030-5912