SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss

ZhaoxinMa; WenjunXia; FeiLiu; JingMa; ShaoyangSun; JinZhang; NanJiang; XuWang; JiongjiongHu; DuanMa

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SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss

机译：SLC44A4突变导致常染色体显性遗传性遗传性缺陷非综合征中频听力损失

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来源
《Human Molecular Genetics》 |2017年第16期|共1页
作者
ZhaoxinMa; WenjunXia; FeiLiu; JingMa; ShaoyangSun; JinZhang; NanJiang; XuWang; JiongjiongHu; DuanMa;
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正文语种 eng
中图分类医学遗传学;
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1. 线粒体功能障碍相关遗传性非综合征型听力损失的研究进展 [J] . 赵晶晶, 汪琪璇, 蔺欣, 中华耳科学杂志（英文版） . 2018,第002期
2. SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss [J] . ZhaoxinMa, WenjunXia, FeiLiu, Human Molecular Genetics . 2017,第16期

机译：SLC44A4突变导致常染色体显性遗传性遗传性缺陷非综合征中频听力损失
3. The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss [J] . Tae-Jun Kwon, Se-Kyung Oh, Hong-Joon Park, Open Biology . 2014,第7期

机译：新突变对与常染色体显性非综合征性听力损失相关的非常规肌球蛋白的结构和酶活性的影响
4. Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations. [J] . Topsakal V, Hilgert N, van Dinther J, Audiology & neuro-otology . 2010,第4期

机译：DFNA22的基因型与表型的相关性：由于MYO6突变导致的非综合征，常染色体显性遗传，进行性感觉神经性听力丧失的特征。
5. DEFECTS IN THE ATP2B2 GENE CAUSING HEREDITARY HEARING AND BALANCE LOSS IN MICE AND HUMANS:A BIOPHYSICAL STUDY OF NORMAL AND MUTATED PMCA2 PUMP FUNCTION [C] . MARIO BORTOLOZZI NATO Advanced Study Institute on Biophotonics: Spectroscopy, Imaging, Sensing, and Manipulation . 2011

机译：ATP2B2基因的缺陷导致遗传性听力和小鼠和人类的失利：正常和突变PMCA2泵功能的生物物理研究
6. Non-syndromic hereditary hearing loss. [D] . Markowitz, Linda Carol. 2002

机译：非综合征性遗传性听力损失。
7. The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss [O] . Tae-Jun Kwon, Se-Kyung Oh, Hong-Joon Park, 2014

机译：新突变对与常染色体显性非综合征性听力损失相关的非常规肌球蛋白的结构和酶活性的影响
8. SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss [O] . Zhaoxin Ma, Wenjun Xia, Fei Liu, 2017

机译：SLC44A4突变导致常染色体显性遗传性遗传性交非综合征中频听力损失

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss

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