Papers

International journal
Jun, 2017

Novel heterozygous deletion mutation c.821delC in the AAA domain of BCS1L underlies Björnstad syndrome.

The Journal of dermatology
  • Yukiko Shigematsu
    • ,
  • Ryota Hayashi
    • ,
  • Kazue Yoshida
    • ,
  • Ai Shimizu
    • ,
  • Masaya Kubota
    • ,
  • Manabu Komori
    • ,
  • Yutaka Shimomura
    • ,
  • Hironori Niizeki
Volume
44
Number
6
First page
e111-e112
Last page
Language
English
Publishing type
DOI
10.1111/1346-8138.13736
Link information
DOI
https://doi.org/10.1111/1346-8138.13736
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28105683
ID information
  • DOI : 10.1111/1346-8138.13736
  • Pubmed ID : 28105683
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