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Analysis of potential biomarkers and modifier genes affecting the clinical course of CLN3 disease. [electronic resource] by
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Non-collagen genes role in digenic Alport syndrome. [electronic resource] by
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Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome. [electronic resource] by
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Epidemiology of ATTRV30M neuropathy in Cyprus and the modifier effect of complement C1q on the age of disease onset. [electronic resource] by
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- Antoniou, Antonis
- Agathangelou, Petros
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Producer: 20190611
In:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis vol. 25
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Neuronatin is a modifier of estrogen receptor-positive breast cancer incidence and outcome. [electronic resource] by
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- Murphy, Dana
- Smith, Jennifer
- Ran, Sophia
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- Hu, Hai
- Mitchell, Edith P
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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease. [electronic resource] by
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In:
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Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics. [electronic resource] by
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- He, Gengming
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- Lin, Fan
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- Gong, Jiafen
- Li, Weili
- Soave, David
- Xiao, Bowei
- Tullis, Elizabeth
- Rabin, Harvey
- Parkins, Michael D
- Price, April
- Zuberbuhler, Peter C
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Human molecular genetics vol. 25
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The Future of Polycystic Kidney Disease Research--As Seen By the 12 Kaplan Awardees. [electronic resource] by
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- Peters, Dorien J M
- Somlo, Stefan
- Torres, Vicente E
- Walz, Gerd
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In:
Journal of the American Society of Nephrology : JASN vol. 26
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The recently identified modifier of murine metastable epialleles, Rearranged L-Myc Fusion, is involved in maintaining epigenetic marks at CpG island shores and enhancers. [electronic resource] by
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- Bharti, Vandhana
- Isbel, Luke
- Daxinger, Lucia
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Producer: 20150914
In:
BMC biology vol. 13
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