Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN
| Title: | Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN |
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| Authors: | Afridi, Tehseen Ullah KhanAff1; Fatima, AmbrinAff2; Satti, Humayoon ShafiqueAff1; Akram, ZainebAff1; Yousafzai, Imran KhanAff1; Naeem, Wajahat BinAff1; Fatima, NasreenAff1; Ali, AsmatAff2; Iqbal, ZafarAff3; Khan, AyazAff4; Shahzad, MuhammadAff5; Liu, ChunyuAff6; Toft, MathiasAff3, Aff7; Zhang, FengAff8; Tariq, MuhammadAff4; Davis, Erica E.Aff9, Aff10, IDs0043802402149y_cor16; Khan, Tahir N.Aff1, Aff9, Aff10, IDs0043802402149y_cor17 |
| Source: | Molecular Genetics and Genomics. 299(1) |
| Database: | Springer Nature Journals |