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Table 1 Primer sequences for Sanger sequencing

From: Analysis of clinical phenotypes and genetic variations in two pedigrees affected with Weiss–Kruszka syndrome

Variation Position

Primer Sequence(5’→3’)

c.6696–2 A > C

F: GCACTTGGACATATATAACGGGT

R: TAGAGGCAGAGAGGACAGCG

c.4891 C > T

F: GTGACCGCTGAGGACTTT

R: CTCGGACATTATTGTGCTTG

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BMC Medical Genomics

ISSN: 1755-8794

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