FREDERICK PEREIRA to Alleles
This is a "connection" page, showing publications FREDERICK PEREIRA has written about Alleles.
Connection Strength
0.145
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An Atoh1-S193A Phospho-Mutant Allele Causes Hearing Deficits and Motor Impairment. J Neurosci. 2017 09 06; 37(36):8583-8594.
Score: 0.101
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An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions. PLoS One. 2013; 8(2):e57460.
Score: 0.019
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DNA sequence analysis of SLC26A5, encoding prestin, in a patient-control cohort: identification of fourteen novel DNA sequence variations. PLoS One. 2009 Jun 02; 4(6):e5762.
Score: 0.014
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High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss. BMC Med Genet. 2005 Aug 08; 6:30.
Score: 0.011