Assessment of French patients with LPL deficiency for French Canadian mutations

Journal of Medical Genetics

Volumn 34, Issue 8, 1997, Pages 672-675

  Foubert, Luc ^a   De Gennes, Jean Luc ^a   Lagarde, Jean Pierre ^a   Ehrenborg, Ewa ^b   Raisonnier, Alain ^a   Girardet, Jean Philippe ^c   Hayden, Michael R ^b   Benlian, Pascale ^b,d  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c ARMAND TROUSSEAU HOSPITAL   (France)

^d HÔPITAL SAINT ANTOINE   (France)

Author keywords

Founder mutation; French Canadians; Lipoprotein lipase

Indexed keywords

LIPOPROTEIN LIPASE;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CANADA; CONTROLLED STUDY; FAMILY; FRANCE; GENE MUTATION; GENETIC HETEROGENEITY; HAPLOTYPE; HUMAN; HUMAN CELL; HYPERLIPOPROTEINEMIA TYPE 1; IMMIGRANT; MAJOR CLINICAL STUDY; MISSENSE MUTATION; PREVALENCE; PRIORITY JOURNAL;

EID: 0030795895     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.8.672     Document Type: Article

References (21)

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