NMNAT1 autosomal recessive disorder: a rare cause of macular scarring.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL

BMJ Case Reports Pub Date : 2024-11-24 DOI:10.1136/bcr-2024-261677

Christopher Stewart, Jaskaran Singh Bhangu, Mahmoud Husseiny Awad, Gwyn Samuel Williams

引用次数: 0

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NMNAT1 常染色体隐性遗传病：黄斑瘢痕的罕见病因。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

BMJ Case Reports Medicine-Medicine (all)

CiteScore

1.40

自引率

0.00%

发文量

1588

期刊介绍： BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.