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

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Corrigendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717922/
https://www.ncbi.nlm.nih.gov/pubmed/26168828
http://dx.doi.org/10.4103/0366-6999.160510
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spelling pubmed-47179222016-04-04 Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum Chin Med J (Engl) Corrigendum Medknow Publications & Media Pvt Ltd 2015-07-20 /pmc/articles/PMC4717922/ /pubmed/26168828 http://dx.doi.org/10.4103/0366-6999.160510 Text en Copyright: © 2015 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Corrigendum
Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum
title Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum
title_full Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum
title_fullStr Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum
title_full_unstemmed Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum
title_short Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome: Corrigendum
title_sort identification of a novel mutation in solute carrier family 29, member 3 in a chinese patient with h syndrome: corrigendum
topic Corrigendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717922/
https://www.ncbi.nlm.nih.gov/pubmed/26168828
http://dx.doi.org/10.4103/0366-6999.160510

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