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A homozygous founder variant in PDE2A causes paroxysmal dys..:
Yousaf, Hammad
;
Rehmat, Shagufta
;
Jameel, Muhammad
...
Clinical Genetics. 104 (2023) 3 - p. 324-333 , 2023
Link:
https://doi.org/10.1111/cge.14386
RT Journal T1
A homozygous founder variant in PDE2A causes paroxysmal dyskinesia with intellectual disability
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14386&Exemplar=1&LAN=DE A1 Yousaf, Hammad A1 Rehmat, Shagufta A1 Jameel, Muhammad A1 Ibrahim, Rabab A1 Hashmi, Sohana Nadeem A1 Makhdoom, Ehtisham Ul Haq A1 Iwaszkiewicz, Justyna A1 Saadi, Saadia Maryam A1 Tariq, Muhammad A1 Baig, Shahid M. A1 Toft, Mathias A1 Fatima, Ambrin A1 Iqbal, Zafar PB Wiley YR 2023 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 104 IS 3 SP 324 OP 333 LK http://dx.doi.org/https://doi.org/10.1111/cge.14386 DO https://doi.org/10.1111/cge.14386 SF ELIB - SuUB Bremen
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