Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nasser Heib"'
Autor:
Hava Peretz, Ayala Lagziel, Florian Bittner, Mustafa Kabha, Meirav Shtauber-Naamati, Vicki Zhuravel, Sali Usher, Steffen Rump, Silke Wollers, Bettina Bork, Hanna Mandel, Tzipora Falik-Zaccai, Limor Kalfon, Juergen Graessler, Avraham Zeharia, Nasser Heib, Hannah Shalev, Daniel Landau, David Levartovsky
Publikováno v:
Biomedicines, Vol 9, Iss 7, p 788 (2021)
Classical xanthinuria is a rare autosomal recessive metabolic disorder caused by variants in the XDH (type I) or MOCOS (type II) genes. Thirteen Israeli kindred (five Jewish and eight Arab) and two isolated cases from Germany were studied between the
Externí odkaz:
https://doaj.org/article/39f61b1380a64273a9863f181879c35b
Autor:
Ayala Lagziel, Avraham Zeharia, Sali Usher, Mustafa Kabha, Nasser Heib, David Levartovsky, Limor Kalfon, Hava Peretz, Bettina Bork, Daniel Landau, Tzipora C Falik-Zaccai, Juergen Graessler, Florian Bittner, Vicki Zhuravel, Silke Wollers, Hannah Shalev, Hanna Mandel, Meirav Shtauber-Naamati, Steffen Rump
Publikováno v:
Biomedicines, Vol 9, Iss 788, p 788 (2021)
Biomedicines
Volume 9
Issue 7
Biomedicines
Volume 9
Issue 7
Classical xanthinuria is a rare autosomal recessive metabolic disorder caused by variants in the XDH (type I) or MOCOS (type II) genes. Thirteen Israeli kindred (five Jewish and eight Arab) and two isolated cases from Germany were studied between the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd2d2424bf74fad899664a3fa013befc
https://www.mdpi.com/2227-9059/9/7/788
https://www.mdpi.com/2227-9059/9/7/788