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A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease.
Hum Mutat. 2000 Jul;16(1):95. doi: 10.1002/1098-1004(200007)16:1<95::AID-HUMU28>3.0.CO;2-H.
Hum Mutat. 2000.
PMID: 10874324
No abstract available.
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.
Zurutuza L, Verpillat P, Raux G, Hannequin D, Puel M, Belliard S, Michon A, Pothin Y, Camuzat A, Penet C, Martin C, Brice A, Campion D, Clerget-Darpoux F, Frebourg T.
Zurutuza L, et al. Among authors: pothin y.
Eur J Hum Genet. 2000 Sep;8(9):713-6. doi: 10.1038/sj.ejhg.5200513.
Eur J Hum Genet. 2000.
PMID: 10980578
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SCA2 is not a major locus for ADCA type I in French families.
Cancel G, Stevanin G, Dürr A, Chneiweiss H, Penet C, Pothin Y, Agid Y, Brice A.
Cancel G, et al. Among authors: pothin y.
Am J Med Genet. 1995 Oct 9;60(5):382-5. doi: 10.1002/ajmg.1320600507.
Am J Med Genet. 1995.
PMID: 8546150
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Common cancer-associated PIK3CA activating mutations rarely occur in Langerhans cell histiocytosis.
Héritier S, Saffroy R, Radosevic-Robin N, Pothin Y, Pacquement H, Peuchmaur M, Lemoine A, Haroche J, Donadieu J, Emile JF.
Héritier S, et al. Among authors: pothin y.
Blood. 2015 Apr 9;125(15):2448-9. doi: 10.1182/blood-2015-01-625491.
Blood. 2015.
PMID: 25858893
Free article.
No abstract available.
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