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Table 1 Primer used in this study. Overhangs with respective restriction sites are highlighted by the use of (*)

From: Whole-genome sequencing, as a powerful diagnostic tool in hearing loss, reveals novel variants in PTPRQ missed by whole-exome sequencing

Primer

Sequence

PTPRQ Ex41 For

ACAATGACGCTTATGACTGATGA

PTPRQ Ex41 Rev

CAGGAGATGAGTGACTTGG

PTPRQ delins Ex43 For

TGCCTTCAACCTTCATTGTGG

PTPRQ delins Ex43 REV

TTATGGTTTTACTGGCCCTGC

PTPRQ MG int23 fw XhoI

*TCATACTCGAG*ATGGAAAACACAAGCAAGCG

PTPRQ MG int23 rev NotI

*ATCATTGCGGCCGC*ACAACCACACTCTAACACACG

PTPRQ MG int23 seq

CAGAAAGAAAGTCATTGTTCCCG

PTPRQ MG XhoI fw

*TCATACTCGAG*TTCATCTAATACTGTGAGTCATC

PTPRQ MG NotI rev

*ATCATTGCGGCCGC*TGTTCAGAAGACAATACAAAAGCA

pSPL3b cam MG seq

ATATCTGGGATCCTGCAGCG

PTPRQ intron 23-F

AGCAGCACCAAGGGAATCTT

PTPRQ intron 23-R

ACCGCTATGCTAAGAGAGCC

SD6

TCTGAGTCACCTGGACAACC

SA2

ATCTCAGTGGTATTTGTGAGC