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FEBS Letters|January 19, 1999
Dopamine D2 receptor dimers in human and rat brainP Zawarynski, T Tallerico, P Seeman, et al.
Biochemical and Biophysical Research Communications|November 27, 1991
Transcription of a human dopamine D5 pseudogeneT Nguyen, R Sunahara, A Marchese, et al.
Clinical Genetics|November 22, 2011
DFNB49 is an important cause of non-syndromic deafness in Czech Roma patients but not in the general Czech populationD Šafka Brožková, J Laštůvková, H Štěpánková, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|February 1, 1993
Schizophrenia: dopamine D1 receptor sequence is normal, but has DNA polymorphismsK Ohara, C Ulpian, P Seeman, et al.
Molecular Pharmacology|July 1, 1988
Dopamine D1 receptors of the calf parathyroid gland: identification and characterizationH B Niznik, E L Fogel, C J Chen, et al.
Journal of Psychiatry & Neuroscience : JPN|October 24, 1998
The human serotonin-7 receptor pseudogene: variation and chromosome locationD Nam, I H Qian, I Kusumi, et al.
European Journal of Neurology|April 16, 2008
A 71-nucleotide deletion in the periaxin gene in a Romani patient with early-onset slowly progressive demyelinating CMTL Baránková, D Sisková, K Hühne, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosisE Mikesová, K Hühne, B Rautenstrauss, et al.
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