10.3205/10HNOD364
Levaya-Smaliak, Anastasiya
Anastasiya
Levaya-Smaliak
Merculova, Elena
Elena
Merculova
Danilenko, Nina
Nina
Danilenko
Frequency of occurrence of recessive 35delG mutation in GJB2 gene in children with sensorineural hearing loss
German Medical Science GMS Publishing House
2010
ConferencePaper
610 Medical sciences; Medicine
Deutsche Gesellschaft Für Hals-Nasen-Ohren-Heilkunde, Kopf- Und Hals-Chirurgie
Kopf- Und Hals-Chirurgie
Deutsche Gesellschaft Für Hals-Nasen-Ohren-Heilkunde
2010-04-22
2010
en
urn:nbn:de:0183-10hnod3648
10hnod364
text/html
81. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf-und Hals
Introduction: A human being is known to have about 100 genes associated with deafness and hearing loss, which are located in both the nucleus and mitochondria. Most commonly detected mutations are those in the GJB2 gene, mononucleotic deletion 35 delG including, which accounts for up to 50% of[for full text, please go to the a.m. URL]
81. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie