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. 2000 May;46(5):585-7.

doi: 10.1136/gut.46.5.585.

The molecular and genetic base of congenital transport defects

Affiliations

PMID: 10764694
PMCID: PMC1727911
DOI: 10.1136/gut.46.5.585

The molecular and genetic base of congenital transport defects

J F Desjeux. Gut. 2000 May.

. 2000 May;46(5):585-7.

doi: 10.1136/gut.46.5.585.

Author

Affiliation

¹ Conservatoire National des Arts et Métiers Paris, France. desjeux@cnam.fr

PMID: 10764694
PMCID: PMC1727911
DOI: 10.1136/gut.46.5.585

No abstract available

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References

1. Pediatr Res. 1980 Feb;14(2):109-12 - PubMed
1. Science. 1999 Aug 27;285(5432):1390-3 - PubMed
1. Nat Genet. 1995 Sep;11(1):76-82 - PubMed
1. Nat Genet. 1996 Jan;12(1):24-30 - PubMed
1. Nat Genet. 1996 Feb;12(2):216-20 - PubMed

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