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    NNT Pseudoexon Activation as a Novel Mechanism for Disease in Two Siblings With Familial Glucocorticoid Deficiency 
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    • NNT Pseudoexon Activation as a Novel Mechanism for Disease in Two Siblings With Familial Glucocorticoid Deficiency
    •   QMRO Home
    • William Harvey Research Institute
    • Centre for Endocrinology
    • NNT Pseudoexon Activation as a Novel Mechanism for Disease in Two Siblings With Familial Glucocorticoid Deficiency
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    NNT Pseudoexon Activation as a Novel Mechanism for Disease in Two Siblings With Familial Glucocorticoid Deficiency

    Volume
    100
    Pagination
    E350 - E354
    DOI
    10.1210/jc.2014-3641
    Journal
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
    Issue
    2
    ISSN
    0021-972X
    Metadata
    Show full item record
    Authors
    Novoselova, TV; Rath, SR; Carpenter, K; Pachter, N; Dickinson, JE; Price, G; Chan, LF; Choong, CS; Metherell, LA
    URI
    http://qmro.qmul.ac.uk/xmlui/handle/123456789/6687
    Collections
    • Centre for Endocrinology [532]
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