TY - JOUR
T1 - Corrigendum to
T2 - 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)
AU - Ranganath, Prajnya
AU - Matta, Divya
AU - Bhavani, Gandham Sri Lakshmi
AU - Wangnekar, Savita
AU - Jain, Jamal Mohammed Nurul
AU - Verma, Ishwar C.
AU - Kabra, Madhulika
AU - Puri, Ratna D.
AU - Danda, Sumita
AU - Gupta, Neerja
AU - Girisha, Katta M.
AU - Sankar, Vaikom H.
AU - Patil, Siddaramappa J.
AU - Devi, Akella Radha Rama
AU - Bhat, Meenakshi
AU - Gowrishankar, Kalpana
AU - Mandal, Kausik
AU - Aggarwal, Shagun
AU - Tamhankar, Parag Mohan
AU - Tilak, Preetha
AU - Phadke, Shubha R.
AU - Dalal, Ashwin
PY - 2017/3/1
Y1 - 2017/3/1
N2 - 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.
AB - 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.
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U2 - 10.1002/ajmg.a.38040
DO - 10.1002/ajmg.a.38040
M3 - Comment/debate
AN - SCOPUS:85011995262
SN - 1552-4825
VL - 173
JO - American Journal of Medical Genetics, Part A
JF - American Journal of Medical Genetics, Part A
IS - 3
ER -
