Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine

Jurgen Jansen; Edith Friesema; Monique Kester; C Milici; M Reeser; A Gruters; TG Barrett; EE Mancilla; J Svensson; JL Wemeau; MHBD Canalli; J Lundgren; ME McEntagart; N Hopper; WFM Arts; Theo Visser

doi:10.1210/jc.2006-2570

Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine

Jurgen Jansen, Edith Friesema, Monique Kester, C Milici, M Reeser, A Gruters, TG Barrett, EE Mancilla, J Svensson, JL Wemeau, MHBD Canalli, J Lundgren, ME McEntagart, N Hopper, WFM Arts, Theo Visser

Research output: Contribution to journal › Article › Academic › peer-review

71 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	2378-2381
Number of pages	4
Journal	Journal of Clinical Endocrinology and Metabolism
Volume	92
Issue number	6
DOIs	https://doi.org/10.1210/jc.2006-2570
Publication status	Published - 2007

Research programs

EMC MM-01-39-03
EMC MM-04-44-02

Access to Document

10.1210/jc.2006-2570

http://hdl.handle.net/1765/35399

Cite this

Jansen, J., Friesema, E., Kester, M., Milici, C., Reeser, M., Gruters, A., Barrett, TG., Mancilla, EE., Svensson, J., Wemeau, JL., Canalli, MHBD., Lundgren, J., McEntagart, ME., Hopper, N., Arts, WFM., & Visser, T. (2007). Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine. Journal of Clinical Endocrinology and Metabolism, 92(6), 2378-2381. https://doi.org/10.1210/jc.2006-2570

@article{333225d65b744deea21eda2fb60478fb,

title = "Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine",

author = "Jurgen Jansen and Edith Friesema and Monique Kester and C Milici and M Reeser and A Gruters and TG Barrett and EE Mancilla and J Svensson and JL Wemeau and MHBD Canalli and J Lundgren and ME McEntagart and N Hopper and WFM Arts and Theo Visser",

year = "2007",

doi = "10.1210/jc.2006-2570",

language = "Undefined/Unknown",

volume = "92",

pages = "2378--2381",

journal = "Journal of Clinical Endocrinology and Metabolism",

issn = "0021-972X",

publisher = "Endocrine Society",

number = "6",

}

Jansen, J, Friesema, E, Kester, M, Milici, C, Reeser, M, Gruters, A, Barrett, TG, Mancilla, EE, Svensson, J, Wemeau, JL, Canalli, MHBD, Lundgren, J, McEntagart, ME, Hopper, N, Arts, WFM & Visser, T 2007, 'Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine', Journal of Clinical Endocrinology and Metabolism, vol. 92, no. 6, pp. 2378-2381. https://doi.org/10.1210/jc.2006-2570

Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine. / Jansen, Jurgen; Friesema, Edith; Kester, Monique et al.
In: Journal of Clinical Endocrinology and Metabolism, Vol. 92, No. 6, 2007, p. 2378-2381.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine

AU - Jansen, Jurgen

AU - Friesema, Edith

AU - Kester, Monique

AU - Milici, C

AU - Reeser, M

AU - Gruters, A

AU - Barrett, TG

AU - Mancilla, EE

AU - Svensson, J

AU - Wemeau, JL

AU - Canalli, MHBD

AU - Lundgren, J

AU - McEntagart, ME

AU - Hopper, N

AU - Arts, WFM

AU - Visser, Theo

PY - 2007

Y1 - 2007

U2 - 10.1210/jc.2006-2570

DO - 10.1210/jc.2006-2570

M3 - Article

C2 - 17356046

SN - 0021-972X

VL - 92

SP - 2378

EP - 2381

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

IS - 6

ER -