Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss
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Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss
description
2018 nî lūn-bûn
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2018年の論文
@ja
2018年学术文章
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2018年学术文章
@zh
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@zh-hans
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@zh-my
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@zh-sg
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name
Whole exome sequencing identif ...... ith non-syndromic hearing loss
@en
type
label
Whole exome sequencing identif ...... ith non-syndromic hearing loss
@en
prefLabel
Whole exome sequencing identif ...... ith non-syndromic hearing loss
@en
P2093
P1433
P1476
Whole exome sequencing identif ...... ith non-syndromic hearing loss
@en
P2093
Alireza Biglari
Majid Changi-Ashtiani
Mohammad Shahrooei
Neda Mohsen-Pour
Somayeh Khatami
Tina Shahani
P304
P356
10.1016/J.MITO.2018.08.006
P577
2018-09-08T00:00:00Z