Corrigendum to “Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families”

المؤلفون المشاركون

Xiao, Yun
Xu, Lei
Bai, Xiaohui
Zhang, Chi
Zhang, Fengguo
Wang, Haibo
Jin, Yu

المصدر

BioMed Research International

العدد

المجلد 2020، العدد 2020 (31 ديسمبر/كانون الأول 2020)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2020-09-29

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الملخص EN

In the article titled “Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families” [1], there were errors in Section 2.3, Section 3.2, footnote of Table 3, and Figure 4.

These errors are shown below:

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Bai, Xiaohui& Zhang, Chi& Zhang, Fengguo& Xiao, Yun& Jin, Yu& Wang, Haibo…[et al.]. 2020. Corrigendum to “Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families”. BioMed Research International،Vol. 2020, no. 2020, pp.1-4.
https://search.emarefa.net/detail/BIM-1138153

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Bai, Xiaohui…[et al.]. Corrigendum to “Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families”. BioMed Research International No. 2020 (2020), pp.1-4.
https://search.emarefa.net/detail/BIM-1138153

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Bai, Xiaohui& Zhang, Chi& Zhang, Fengguo& Xiao, Yun& Jin, Yu& Wang, Haibo…[et al.]. Corrigendum to “Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families”. BioMed Research International. 2020. Vol. 2020, no. 2020, pp.1-4.
https://search.emarefa.net/detail/BIM-1138153

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1138153