BICD2引起的常染色体显性遗传性脊髓性肌萎缩的声带麻痹。

IF 1.3 4区医学 Q3 PEDIATRICS

Congenital Anomalies Pub Date : 2022-12-14 DOI:10.1111/cga.12500

Sachiko Matsui, Sota Iwatani, Naoya Morisada, Toshiki Takenouchi, Seiji Yoshimoto

引用次数: 0

摘要

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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Vocal cord paralysis in autosomal dominant spinal muscular atrophy due to BICD2

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来源期刊

Congenital Anomalies PEDIATRICS-

自引率

0.00%

发文量

审稿时长

>12 weeks

期刊介绍： Congenital Anomalies is the official English language journal of the Japanese Teratology Society, and publishes original articles in laboratory as well as clinical research in all areas of abnormal development and related fields, from all over the world. Although contributions by members of the teratology societies affiliated with The International Federation of Teratology Societies are given priority, contributions from non-members are welcomed.