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Academic Journal

Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities.

  • Authors : Li W; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, M5T 3M7, Canada, .; Soave D

Subjects: Cystic Fibrosis/Cystic Fibrosis/Cystic Fibrosis/*genetics ; Cystic Fibrosis Transmembrane Conductance Regulator/Cystic Fibrosis Transmembrane Conductance Regulator/Cystic Fibrosis Transmembrane Conductance Regulator/*genetics ; Genes, Modifier/Genes, Modifier/Genes, Modifier/*genetics

  • Source: Human genetics [Hum Genet] 2014 Feb; Vol. 133 (2), pp. 151-61. Date of Electronic Publication: 2013 Sep 22.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Molecular analysis of cystinosis: probable Irish origin of the most common French Canadian mutation.

Subjects: Glycoproteins* ; Mutation*; Cystinosis/Cystinosis/Cystinosis/*genetics

  • Source: European journal of human genetics : EJHG [Eur J Hum Genet] 1999 Sep; Vol. 7 (6), pp. 671-8.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813

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  • 1-2 of  2 results for ""Amino Acid Transport Systems, Neutral""