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3338.
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GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemia. [electronic resource] by
- Charrière, Sybil
- Peretti, Noël
- Bernard, Sophie
- Di Filippo, Mathilde
- Sassolas, Agnès
- Merlin, Micheline
- Delay, Mireille
- Debard, Cyrille
- Lefai, Etienne
- Lachaux, Alain
- Moulin, Philippe
- Marçais, Christophe
Producer: 20111118
In:
The Journal of clinical endocrinology and metabolism vol. 96
Availability: No items available.
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3339.
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3340.
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