Corrigendum to: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817)

Prajnya Ranganath, Divya Matta, Gandham Sri Lakshmi Bhavani, Savita Wangnekar, Jamal Mohammed Nurul Jain, Ishwar C. Verma, Madhulika Kabra, Ratna D. Puri, Sumita Danda, Neerja Gupta, Katta M. Girisha, Vaikom H. Sankar, Siddaramappa J. Patil, Akella Radha Rama Devi, Meenakshi Bhat, Kalpana Gowrishankar, Kausik Mandal, Shagun Aggarwal, Parag Mohan Tamhankar, Preetha TilakShubha R. Phadke, Ashwin Dalal*

*Corresponding author for this work

Research output: Contribution to journalComment/debatepeer-review

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Abstract

Authors Ashwin Dalal This article corrects: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease, Am J Med Genet A. 2016 Oct; Volume 170A, Issue 10, 2719–2730, Article first published online: June 24 2016. There was an error in the mutation description of the patient number 59 in Table I reported in this article. The correct mutation description in this patient with Niemann Pick disease Type A is NG_011780.1: g.8462_8560dup (and not NG_011780.1:g.3471_3570dup). Dr. Andrew Phillips, Research Associate, Human Gene Mutation Database, UK detected this mistake when reviewing the mutations in patients with this disease for the database. I am grateful that he informed us about this, and that this can be corrected now.

Original languageEnglish
Pages (from-to)829
Number of pages1
JournalAmerican Journal of Medical Genetics, Part A
Volume173
Issue number3
DOIs
Publication statusPublished - Mar 1 2017

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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