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Andrew Orr

Dalhousie University
H指数:18
被引数:1,788

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Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosis
2024-04-013
OA
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye

罕见的CYP39A1变异体与涉及眼睛前房的剥脱综合征的关联

2021-02-2321
OA
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

剥脱综合征的遗传关联研究确定了LOXL1的保护性罕见变异和五个新的易感位点

2017-05-29107
OAAI
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome (vol 47, pg 387, 2015)

CACNA1A的常见变异与剥脱综合征的易感性相关 (第47卷,387页,2015页)

2015-05-271
OAAI
Germline Mutations in MAP3K6 Are Associated with Familial Gastric Cancer
2014-10-2355
OAAI
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
2011-02-27159
PREAI
Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4
2010-07-01173
OAAI
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
2009-05-03211
PREAI