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    Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency 
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    • Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
    •   QMRO Home
    • William Harvey Research Institute
    • Centre for Endocrinology
    • Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
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    Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency

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    Published version (147.3Kb)
    Volume
    71
    Pagination
    171 - 175
    DOI
    10.1111/j.1365-2265.2008.03511.x
    Journal
    CLIN ENDOCRINOL
    Issue
    2
    ISSN
    0300-0664
    Metadata
    Show full item record
    Authors
    Chan, LF; Metherell, LA; Krude, H; Ball, C; O'Riordan, SMP; Costigan, C; Lynch, SA; Savage, MO; Cavarzere, P; Clark, AJL
    URI
    http://qmro.qmul.ac.uk/xmlui/handle/123456789/18040
    Collections
    • Centre for Endocrinology [527]
    Licence information
    Creative Commons Deed, Attribution 2·5, which does not permit commercial exploitation.
    Copyright statements
    2009. The authors
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