Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain
Esra Yıldız Bölükbaşı; Muhammad Afzal; Sara Mumtaz; Nafees Ahmad; Sajid Malik; Aslıhan Tolun
Author Information: Department of Molecular Biology and Genetics
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