Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.

Translated title of the contribution: Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.

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Translated title of the contribution	Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.
Original language	Undefined/Unknown
Pages (from-to)	808-814
Number of pages	7
Journal	Clinical Endocrinology
Volume	73
Issue number	6
Publication status	Published - 2010

Cite this

@article{306cf46a8804446facd844d24bd9cff1,

title = "Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.",

author = "\{Di Palma\}, T. and E. Zampella and M.G. Filippone and P.E. Macchia and C. Ris-Stalpers and \{de Vroede\}, M. and M. Zannini",

year = "2010",

language = "Undefined/Unknown",

volume = "73",

pages = "808--814",

journal = "Clinical Endocrinology",

issn = "0300-0664",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "6",

}

TY - JOUR

T1 - Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.

AU - Di Palma, T.

AU - Zampella, E.

AU - Filippone, M.G.

AU - Macchia, P.E.

AU - Ris-Stalpers, C.

AU - de Vroede, M.

AU - Zannini, M.

PY - 2010

Y1 - 2010

M3 - Article

SN - 0300-0664

VL - 73

SP - 808

EP - 814

JO - Clinical Endocrinology

JF - Clinical Endocrinology

IS - 6

ER -