reference/10078983

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10078983

Outgoing Links

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bibliographicCitation	Logan C, Cossins J, Rodríguez Cruz P, Parry D, Maxwell S, Martínez-Martínez P, Riepsaame J, Abdelhamed Z, Lake AR, Moran M, Robb S, Chow G, Sewry C, Hopkins P, Sheridan E, Jayawant S, Palace J, Johnson C, Beeson D. Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. The American Journal of Human Genetics. 2015 Dec;97(6):878–85. doi: 10.1016/j.ajhg.2015.10.017.
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date	2015-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC4678414 https://doi.org/10.1016/j.ajhg.2015.10.017 https://pubmed.ncbi.nlm.nih.gov/26626625
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain
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