Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondylo­epiphyseal dysplasia congenita

Title
Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondylo­epiphyseal dysplasia congenita
Authors
Keywords
-
Journal
GENETICS AND MOLECULAR RESEARCH
Volume 15, Issue 1, Pages -
Publisher
Genetics and Molecular Research
Online
2016-03-14
DOI
10.4238/gmr.15017624

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