https://www.selleckchem.com/
Dispite the lack the direct proof from the lost fetuses, the variants of ALPL and CDKN1C genes can explain the recurrence of fetal malformations for both couples. To explore the genetic basis of a Chinese pedigree affected with progressive non-syndromic sensorineural hearing loss. High-throughput DNA sequencing was carried out to analyze 415 genes associated with hereditary deafness in the proband. Sanger sequencing was carried out to verify the suspected variants among her family members. The proband was found to carry a heterozygous c.842TA (p.Ile281A
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