Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutation

To report the hearing impairment in a new autosomal recessive metabolic disorder due to a mutation in the ANKH gene and to report the outcomes of exploratory tympanotomy.

Gespeichert in:
Autor*in:

Thomeer, H.G.X.M. [verfasserIn]

Morava, E.

Verbist, B.M.

Cremers, C.W.R.J.

Format:

E-Artikel

Sprache:

Englisch

Erschienen:

2013

Schlagwörter:

Congenital

ANKH

Surgery

Minor ear anomalies

Hearing impairment

Syndrome

Umfang:

6

Übergeordnetes Werk:

Enthalten in: Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study - Reyaz, Saima ELSEVIER, 2021, Amsterdam [u.a.]

Übergeordnetes Werk:

volume:77 ; year:2013 ; number:7 ; pages:1152-1157 ; extent:6

Links:

Volltext

DOI / URN:

10.1016/j.ijporl.2013.04.028

Katalog-ID:

ELV027092984

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