OTOF mutation screening in Japanese severe to profound recessive hearing loss patients

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2350

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: OTOF mutation screening in Japanese severe to profound recessive hearing loss patients ; volume:14 ; number:1 ; day:22 ; month:9 ; year:2013 ; pages:1-7 ; date:12.2013
BMC medical genetics ; 14, Heft 1 (22.9.2013), 1-7, 12.2013

Creator: Iwasa, Yoh-ichiro

Contributor: Nishio, Shin-ya
Yoshimura, Hidekane
Kanda, Yukihiko
Kumakawa, Kozo
Abe, Satoko
Naito, Yasushi
Nagai, Kyoko
Usami, Shin-ichi
SpringerLink (Online service)

DOI: 10.1186/1471-2350-14-95

URN: urn:nbn:de:1111-2016071516235

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:51 AM CEST

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Iwasa, Yoh-ichiro
Nishio, Shin-ya
Yoshimura, Hidekane
Kanda, Yukihiko
Kumakawa, Kozo
Abe, Satoko
Naito, Yasushi
Nagai, Kyoko
Usami, Shin-ichi
SpringerLink (Online service)

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OTOF mutation screening in Japanese severe to profound recessive hearing loss patients

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Other Objects (12)

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

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Evaluation of vestibular system in profound sensorineural hearing loss patients

A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss

Vestibular function following unilateral cochlear implantation for profound sensorineural hearing loss

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

A novel mutation in 3’UTR of GJB2 gene in autosomal recessive nonsyndromic sensorineural hearing loss in South Indian population

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract

Hearing-impaired seniors with profound hearing loss: Too many with inadequate hearing aid fitting!

Recessive TMOD1 mutation causes childhood cardiomyopathy

Evaluation of vestibular system in profound sensorineural hearing loss patients

A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

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