This page shows the publications Kevin Booth has written about Alleles.
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment. J Med Genet. 2018 08; 55(8):555-560.
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. Hum Genet. 2021 Jun; 140(6):915-931.
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.