Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

MA Kurian; Y Li; J Zhen; E Meyer; NA Hai; HJ Christen; GF Hoffmann; PE Jardine; A von Moers; SR Mordekar; FJK O'Callaghan; E Wassmer; E Wraige; C Dietrich; T Lewis; K Hyland; SJ Heales; T Sanger; P Gissen; BE Assmann; ME Reith; ER Maher

doi:10.1016/S1474- 4422(10)70269-6

Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

MA Kurian, Y Li, J Zhen, E Meyer, NA Hai, HJ Christen, GF Hoffmann, PE Jardine, A von Moers, SR Mordekar, FJK O'Callaghan, E Wassmer, E Wraige, C Dietrich, T Lewis, K Hyland, SJ Heales, T Sanger, P Gissen, BE AssmannME Reith, ER Maher

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Translated title of the contribution	Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
Original language	English
Pages (from-to)	24 - 25
Journal	Lancet Neurology
Volume	10(1)
DOIs	https://doi.org/10.1016/S1474- 4422(10)70269-6
Publication status	Published - Jan 2011

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Kurian, MA., Li, Y., Zhen, J., Meyer, E., Hai, NA., Christen, HJ., Hoffmann, GF., Jardine, PE., von Moers, A., Mordekar, SR., O'Callaghan, FJK., Wassmer, E., Wraige, E., Dietrich, C., Lewis, T., Hyland, K., Heales, SJ., Sanger, T., Gissen, P., ... Maher, ER. (2011). Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study. Lancet Neurology, 10(1), 24 - 25. https://doi.org/10.1016/S1474- 4422(10)70269-6

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title = "Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study",

author = "MA Kurian and Y Li and J Zhen and E Meyer and NA Hai and HJ Christen and GF Hoffmann and PE Jardine and {von Moers}, A and SR Mordekar and FJK O'Callaghan and E Wassmer and E Wraige and C Dietrich and T Lewis and K Hyland and SJ Heales and T Sanger and P Gissen and BE Assmann and ME Reith and ER Maher",

year = "2011",

month = jan,

doi = "10.1016/S1474- 4422(10)70269-6",

language = "English",

volume = "10(1)",

pages = "24 -- 25",

journal = "Lancet Neurology",

issn = "1474-4465",

publisher = "Lancet Publishing Group",

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Kurian, MA, Li, Y, Zhen, J, Meyer, E, Hai, NA, Christen, HJ, Hoffmann, GF, Jardine, PE, von Moers, A, Mordekar, SR, O'Callaghan, FJK, Wassmer, E, Wraige, E, Dietrich, C, Lewis, T, Hyland, K, Heales, SJ, Sanger, T, Gissen, P, Assmann, BE, Reith, ME & Maher, ER 2011, 'Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study', Lancet Neurology, vol. 10(1), pp. 24 - 25. https://doi.org/10.1016/S1474- 4422(10)70269-6

TY - JOUR

T1 - Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

AU - Kurian, MA

AU - Li, Y

AU - Zhen, J

AU - Meyer, E

AU - Hai, NA

AU - Christen, HJ

AU - Hoffmann, GF

AU - Jardine, PE

AU - von Moers, A

AU - Mordekar, SR

AU - O'Callaghan, FJK

AU - Wassmer, E

AU - Wraige, E

AU - Dietrich, C

AU - Lewis, T

AU - Hyland, K

AU - Heales, SJ

AU - Sanger, T

AU - Gissen, P

AU - Assmann, BE

AU - Reith, ME

AU - Maher, ER

PY - 2011/1

Y1 - 2011/1

U2 - 10.1016/S1474- 4422(10)70269-6

DO - 10.1016/S1474- 4422(10)70269-6

M3 - Article (Academic Journal)

SN - 1474-4465

VL - 10(1)

SP - 24

EP - 25

JO - Lancet Neurology

JF - Lancet Neurology

ER -