Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan.

Vincent, J B;Jamil, T;Rafiq, M A;Anwar, Z;Ayub, M;et.al.
(2015) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 87, n° 3, p. 296-298 (2015)

Files

document.pdf
  • Restricted Access
  • Adobe PDF
  • 872.82 KB

Details

Authors
  • Vincent, J B
    Author
  • Jamil, T
    Author
  • Rafiq, M A
    Author
  • Anwar, Z
    Author
  • Wiame, ElsaUCLouvain
    Author
  • Author
  • Ayub, M
    Author
Show more
Affiliations

Citations

Vincent, J. B., Jamil, T., Rafiq, M. A., Anwar, Z., Ayaz, M., Hameed, A., Nasr, T., Naeem, F., Khattak, N. A., Carter, M., Ahmed, I., John, P., Wiame, E., Andrade, D. M., Van Schaftingen, E., Mir, A., & Ayub, M. (2015). Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan. Clinical Genetics : an international journal of genetics and molecular medicine, 87(3), 296-298. https://doi.org/10.1111/cge.12445 (Original work published 2015)