Developmental window of sensorineural deafness in biotinidase-deficient mice
Author:
Funder
National Multiple Sclerosis Society
National Institutes of Health (US)
Safra Research Fund
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/article/10.1007/s10545-017-0049-z/fulltext.html
Reference48 articles.
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3. Boison D, Stoffel W (1994) Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice. Proc Natl Acad Sci U S A 91:11709–11713
4. Box GEP, Cox DR (1964) An analysis of transformations. J Royal Stat Soc, Series B 26:211–252
5. Brumwell CL, Hossain WA, Morest DK, Wolf B (2005) Biotinidase reveals the morphogenetic sequence in cochlea and cochlear nucleus of mice. Hear Res 209:104–121
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1. Alterações auditivas e deficiência de biotinidase: revisão integrativa da literatura;Revista CEFAC;2022
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3. The novel homozygous p.Asn197_Ser201del mutation in BTD gene is associated with profound biotinidase deficiency in an Iranian consanguineous family;Molecular Biology Reports;2020-04-12
4. Biotin;Present Knowledge in Nutrition;2020
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