All individuals with variants in gene SLC6A3

13 entries on 1 page. Showing entries 1 - 13.
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00117474 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Esther Meyer
00117475 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 2 1 Esther Meyer
00117476 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Esther Meyer
00117477 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 3 1 Esther Meyer
00117478 - PubMed: Kurian 2010 - - - Turkey Turkish - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Esther Meyer
00117479 - PubMed: Kurian 2009 - - - Pakistan Pakistani - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Johan den Dunnen
00117480 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Johan den Dunnen
00117481 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Derek Lim
00117482 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Esther Meyer
00117483 - PubMed: Kurian 2010 - - - - European, mixed - 0 - - PKDYS1;DTDS Dopamine Transporter deficiency syndrome 1 1 Esther Meyer
00117484 - PubMed: Mazei-Robison 2005 ADHD Patient - - - - - 0 - - ADHD attention-deficit hyperactivity disorder 1 1 Esther Meyer
00265597 DTDS-SLC6A3 PubMed: Heidari 2020 4-generation family, 2 affected, unaffected heterozygous carrier parents/relatives F yes Iran Persian - 0 - - PKDYS1;DTDS HP:0002015, HP:0002355, HP:0000750, HP:0002355, HP:0002015, HP:0002141, HP:0001347, HP:0000737, HP:0002451 1 1 Ehsan Razmara
00408972 1 PubMed: Puffenberger 2012 no patient number in publication, consecutive numbers given ? - - Old Order Amish and Mennonite - 0 - - PKDYS1;DTDS infantile-onset rigidity, dystonia, or chorea; dopamine non-responsive parkinsonism; progressive frontal lobe degeneration 1 1 LOVD
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