Non-syndromic isolated dominant optic atrophy caused by the p.R468C mutation in the AFG3 like matrix AAA peptidase subunit 2 gene.
about
Non-syndromic isolated dominant optic atrophy caused by the p.R468C mutation in the AFG3 like matrix AAA peptidase subunit 2 gene.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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name
Non-syndromic isolated dominan ...... AAA peptidase subunit 2 gene.
@en
Non-syndromic isolated dominan ...... AAA peptidase subunit 2 gene.
@nl
type
label
Non-syndromic isolated dominan ...... AAA peptidase subunit 2 gene.
@en
Non-syndromic isolated dominan ...... AAA peptidase subunit 2 gene.
@nl
prefLabel
Non-syndromic isolated dominan ...... AAA peptidase subunit 2 gene.
@en
Non-syndromic isolated dominan ...... AAA peptidase subunit 2 gene.
@nl
P2093
P2860
P356
P1433
P1476
Non-syndromic isolated dominan ...... x AAA peptidase subunit 2 gene
@en
P2093
Alberta Leon
Davide Colavito
Elda Del Giudice
Maurizio Dalle Carbonare
Monica Mazzarolo
Sofia Farina
Stefania Miotto
Stefano Piermarocchi
Veronica Maritan
P2860
P304
P356
10.3892/BR.2017.987
P50
P577
2017-09-22T00:00:00Z