Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mossafa, Houssein"'
Autor:
chbel faiza, charoute hicham, Boulouiz redouane, Hamdaoui Hasna, Mossafa Houssein, Benrahma houda, Karim Ouldim
Myoclonus-Dystonia is a neuropsychiatric disorder with autosomal dominant mode of inheritance with variable severity and incomplete penetrance. Pathogenic variants in SGCE are the most frequent genetic cause of M-D with maternal imprinting. Herein we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3db45d771358a7f958d6efd205fcd3a6
https://doi.org/10.22541/au.163254136.66611445/v1
https://doi.org/10.22541/au.163254136.66611445/v1
Autor:
Chbel, Faiza1,2 (AUTHOR) cfaiza75@gmail.com, Hamdaoui, Hasna1 (AUTHOR), Mossafa, Houssein1 (AUTHOR), Ouldim, Karim1 (AUTHOR), Benrahma, Houda1,3 (AUTHOR)
Publikováno v:
Egyptian Journal of Medical Human Genetics. 3/23/2024, Vol. 25 Issue 1, p1-6. 6p.
Autor:
Chbel, Faiza, Charroute, Hicham, Boulouiz, Redouane, Hamdaoui, Hasna, Mossafa, Houssein, Benrahma, Houda, Ouldim, Karim
Publikováno v:
Clinical Case Reports; Mar2022, Vol. 10 Issue 3, p1-6, 6p