Genetic deafness of central origin-Reference-Cited by-同舟云学术

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Genetic deafness of central origin

Published:1983-01 Issue:1 Volume:258 Page:177-179
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Deol M.S.,Frank Marius P.,Steel Karen P.,Bock Gregory R.

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference12 articles.

1. Inherited diseases of the inner ear in man in the light of studies on the mouse;Deol;J. med. Genet.,1968

2. The relationship between abnormalities of pigmentation and of the inner ear;Deol,1970

3. The ear;Deol,1973

4. Genetic malformations of the inner ear in the mouse and in man;Deol;Birth Defects: Original Article Series,1980

5. The Causes of Profound Deafness in Childhood;Fraser,1976

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Loss of β4-spectrin impairs Nav channel clustering at the heminode and temporal fidelity of presynaptic spikes in developing auditory brain;Scientific Reports;2022-04-07

2. A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness;Human Genetics;2017-05-24

3. Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder;Hearing Research;2015-12

4. Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice;Nature Genetics;2001-08-20

5. The Gene Encoding the Schwann Cell Protein Periaxin Localizes on Mouse Chromosome 7 (Prx);Genomics;1997-04

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