Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6. (Q33945290)

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English	Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

30 July 2017

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Europe PubMed Central

Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6. (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Gilbert B

1

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Europe PubMed Central

PubMed publication ID

30 July 2017

Rouis M

2

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Europe PubMed Central

PubMed publication ID

30 July 2017

Griglio S

3

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Europe PubMed Central

PubMed publication ID

30 July 2017

de Lumley L

4

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Europe PubMed Central

PubMed publication ID

30 July 2017

Laplaud P

5

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Europe PubMed Central

PubMed publication ID

30 July 2017

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1 January 2001

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Europe PubMed Central

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30 July 2017

Annales de Génétique

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Europe PubMed Central

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30 July 2017

44

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Europe PubMed Central

PubMed publication ID

30 July 2017

1

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Europe PubMed Central

PubMed publication ID

30 July 2017

25-32

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Europe PubMed Central

PubMed publication ID

30 July 2017

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10.1016/S0003-3995(01)01037-1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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