Audiological and radiological characteristics of a family with T961G mitochondrial mutation.

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Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment.

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Q35540619-DCF6F5D1-A674-4747-92ED-4FFBE2D4736E

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Audiological and radiological characteristics of a family with T961G mitochondrial mutation.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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name

Audiological and radiological ...... T961G mitochondrial mutation.

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Audiological and radiological ...... T961G mitochondrial mutation.

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Audiological and radiological ...... T961G mitochondrial mutation.

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Audiological and radiological ...... T961G mitochondrial mutation.

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Audiological and radiological ...... T961G mitochondrial mutation.

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Audiological and radiological ...... T961G mitochondrial mutation.

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Audiological and radiological ...... T961G mitochondrial mutation.

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Alessandro Ferraris

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Chiara de Vincentiis

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Daniela Messineo

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Ferdinando D'Ambrosio

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Filippo Mazzei

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Giancarlo Altissimi

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Giancarlo Cianfrone

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Maria Gloria Cammeresi

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Maria Patrizia Orlando

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Rosaria Turchetta

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Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

Mitochondrial defects and hearing loss.

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Enlarged vestibular aqueduct: Looking for genotypic-phenotypic correlations.

The large vestibular aqueduct: a new definition based on audiologic and computed tomography correlation.

Clinical aspects of hereditary hearing loss.

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

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870-879

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scholarly article

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10.3109/14992027.2012.712721

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2012-09-27T00:00:00Z

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23013294

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Audiological and radiological characteristics of a family with T961G mitochondrial mutation.

about

P2860

P2860

Audiological and radiological characteristics of a family with T961G mitochondrial mutation.

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P1476

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P433

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