Literature DB >> 26168828

Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum.

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Abstract

Entities:  

Year:  2015        PMID: 26168828      PMCID: PMC4717922          DOI: 10.4103/0366-6999.160510

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


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In the article, “Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome”, which appeared in the pages 1336-1339, Issue 10, Vol 128 of Chinese Medical Journal[1], the word “c. 1269_1270delinsA” in the whole article should be written as “c.1269_1270delinsT”. In the paragraph under the section “Identification of a novel mutation in solute carrier family 29, member 3” the word “p.Leu423Serfs*28” in first and fourth sentence should be written as “p.Leu424Serfs*29”. Additionally, in the sentence “This indel (c. 1269_1270delinsA) changed leucine 423 to serine and was predicted to result in a frameshift and the generation of a stop codon at residue 451 of the protein, which will disrupt the 10th and delete 11th TMD of SLC29A3, leads to the dysfunction of the hENT3 and presents a series of clinical disorders.” on page 1338 the numbers “423” and “451” should be written as “424” and “453” respectively. These have now been corrected and reposted online
  1 in total

1.  Identification of a novel mutation in solute carrier family 29, member 3 in a Chinese patient with H syndrome.

Authors:  Jia-Wei Liu; Nuo Si; Lian-Qing Wang; Ti Shen; Xue-Jun Zeng; Xue Zhang; Dong-Lai Ma
Journal:  Chin Med J (Engl)       Date:  2015-05-20       Impact factor: 2.628

  1 in total

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