Erratum to "Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCR" [Neuromuscular Disorders, 30(3) 2020, 219-226].

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Title: Erratum to "Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCR" [Neuromuscular Disorders, 30(3) 2020, 219-226].
Authors: Xu Y; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Xiao B; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Liu Y; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Qu XX; Department of Fetal Medicine Center, Shanghai First Maternity and Infant Hospital Affiliated to Shanghai Tongji University, Shanghai, China., Dai MY; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Ying XM; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Jiang WT; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Zhang JM; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Liu XQ; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China; Department of Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Shanghai, China., Chen YW; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China., Ji X; Department of Genetic Counseling, Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China. Electronic address: jixing@xinhuamed.com.cn.
Source: Neuromuscular disorders : NMD [Neuromuscul Disord] 2021 Jan; Vol. 31 (1), pp. e1. Date of Electronic Publication: 2020 Dec 01.
Publication Type: Published Erratum
Journal Info: Publisher: Pergamon Press Country of Publication: England NLM ID: 9111470 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2364 (Electronic) Linking ISSN: 09608966 NLM ISO Abbreviation: Neuromuscul Disord Subsets: MEDLINE; PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1873-2364
DOI:10.1016/j.nmd.2020.11.006