Assessment of French patients with LPL deficiency for French Canadian mutations.

Mutations in the LPL gene show high levels of allelic heterogeneity between and within different populations. Complete LPL deficiency has a very high prevalence in French Canadians, where only three missense mutations account for > 97% of cases, most consistent with founder mutations introduced e...

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Bibliografiske detaljer
Main Authors: Foubert, L, De Gennes, J L, Lagarde, J P, Ehrenborg, E, Raisonnier, A, Girardet, J P, Hayden, M R, Benlian, P
Format: Artigo
Sprog:Inglês
Udgivet: 1997
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051031/
https://ncbi.nlm.nih.gov/pubmed/9279761
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