Asmat Ullah

Asmat Ullah

Postdoc


Publication year:
All
  1. 2021
  2. E-pub ahead of print

    Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous Families

    Nawal, W., Ullah, Asmat, Ullah, U., Farrakh, K., Ahmad, F., Khan, H., Ahmad, G. S., Khan, B., Ansar, M., Umm-e-Kalsoom & Ahmad, W., Sep 2021, (E-pub ahead of print) In: Klinische Padiatrie. 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. E-pub ahead of print

    ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment

    Bharadwaj, T., Schrauwen, I., Rehman, S., Liaqat, K., Acharya, A., Giese, A. P. J., Nouel-Saied, L. M., Nasir, A., Everard, J. L., Pollock, L. M., Zhu, S., Bamshad, M. J., Nickerson, D. A., Ali, R. H., Ullah, Asmat, Wali, A., Ali, G., Santos-Cortez, R. L. P., Ahmed, Z. M., McDermott, B. M., Ansar, M., Riazuddin, S., Ahmad, W. & Leal, S. M., 2021, (E-pub ahead of print) In: European Journal of Human Genetics.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 249147337