Pediatrics and Neonatology (Jun 2018)

Identification of one novel homozygous mutation in the NPR2 gene in a patient from Taiwan with acromesomelic dysplasia Maroteaux type

  • Wei-De Lin,
  • Chung-Hsing Wang,
  • Fuu-Jen Tsai

DOI
https://doi.org/10.1016/j.pedneo.2017.11.017
Journal volume & issue
Vol. 59, no. 3
pp. 322 – 323

Abstract

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