Novel mutation s.7348C>T in NF1 gene identified by wholeexome sequencing in patient with overlapping clinical symptoms of neurofibromatosis type 1 and bannayanrileyruvalcaba syndrome / Rahmani, E. S., Azarpara, H., Abazari, M. F., Mohajeri, M. R., Nasimi, M., Ghorbani, R., Azizpour, A., Rahimi, H. (2020)
web address of the page http://jnas.nbuv.gov.ua/article/UJRN-0001166407
Cytology and genetics   А - 2019 /  Issue (2020, Т. 54, № 4)
Rahmani E. S., Azarpara H., Abazari M. F., Mohajeri M. R., Nasimi M., Ghorbani R., Azizpour A., Rahimi H.
Novel mutation с.7348C>T in NF1 gene identified by wholeexome sequencing in patient with overlapping clinical symptoms of neurofibromatosis type 1 and bannayanrileyruvalcaba syndrome
Cite:
Rahmani, E. S., Azarpara, H., Abazari, M. F., Mohajeri, M. R., Nasimi, M., Ghorbani, R., Azizpour, A., Rahimi, H. (2020). Novel mutation s.7348C>T in NF1 gene identified by wholeexome sequencing in patient with overlapping clinical symptoms of neurofibromatosis type 1 and bannayanrileyruvalcaba syndrome. Cytology and genetics, 54 (4), 87-89. http://jnas.nbuv.gov.ua/article/UJRN-0001166407 | |
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