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Publications by Connie Lund
Similar Splice-Site Mutations of the ATP7A Gene Lead to Different Phenotypes: Classical Menkes Disease or Occipital Horn Syndrome
American Journal of Human Genetics
Genetics
Evidence That Translation Reinitiation Leads to a Partially Functional Menkes Protein Containing Two Copper-Binding Sites
American Journal of Human Genetics
Genetics
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From Lowe Syndrome to Dent Disease: Correlations Between Mutations of the OCRL1 Gene and Clinical and Biochemical Phenotypes
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Novel NPHS1 Splice Site Mutations in a Chinese Child With Congenital Nephrotic Syndrome
Genetics and Molecular Research
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ATP7A (Menkes Protein) Functions in Axonal Targeting and Synaptogenesis
Molecular and Cellular Neurosciences
Molecular Neuroscience
Molecular Biology
Cell Biology
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Caveolin-3 T78M and T78K Missense Mutations Lead to Different Phenotypes in Vivo and in Vitro
Laboratory Investigation
Forensic Medicine
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Novel Splice Site IDUA Gene Mutation in Tunisian Pedigrees With Hurler Syndrome
Diagnostic Pathology
Forensic Medicine
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Histology
A Single PDZ Domain Protein Interacts With the Menkes Copper ATPase, ATP7A
Journal of Biological Chemistry
Biochemistry
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Molecular Biology
Inflammatory Bowel Disease in Japan-Is It Similar to or Different From Westerns?-
Journal of the Anus, Rectum and Colon
Expression of Menkes Disease Gene in Mammary Carcinoma Cells
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes
Frontiers in Genetics
Genetics
Molecular Medicine
