HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

@en

HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

@en

HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

@nl

P1476

HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients

@en

P2093

Ali Bouslama

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Asma Omezzine

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Cécile Aquaviva-Bourdain

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Geneviéve Souche

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Ibtihel M'barek

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Saoussen Abroug

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Saoussen M'dimegh

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Tahar Gargah

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P2860

The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II

Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria

Mutations in DHDPSL are responsible for primary hyperoxaluria type III

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis

Primary hyperoxaluria.

Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.

Primary hyperoxaluria type 1: still challenging!

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

An update on primary hyperoxaluria.

P31

scholarly article

P356

10.1002/JCLA.22053

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P433

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P478

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P50

Kamel Abidi

P577

2016-08-26T00:00:00Z

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P698

27561601

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P932

6817302

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