Exome sequencing identifies homozygous variants in MBOAT7 associated with neurodevelopmental disorder

Nazmina, Gul; Khan, Amjad; Jiang, Jiuhong; Miao, Zhichao; Khan, Shahid Niaz; Khan, Muhammad Ismail; Shah, Abdul Haleem; Shah, Aysha Haleem; Khisroon, Muhammad; Haack, Tobias B.

dc.contributor.author	Khan, Amjad
dc.contributor.author	Haack, Tobias
dc.date.accessioned	2024-08-26T07:56:25Z
dc.date.available	2024-08-26T07:56:25Z
dc.date.issued	2024
dc.identifier.issn	0009-9163
dc.identifier.uri	http://hdl.handle.net/10900/157041
dc.language.iso	en	de_DE
dc.publisher	Hoboken : Wiley	de_DE
dc.relation.uri	http://dx.doi.org/10.1111/cge.14469	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Exome sequencing identifies homozygous variants in MBOAT7 associated with neurodevelopmental disorder	de_DE
dc.type	Article	de_DE
utue.quellen.id	20240422000000_01242
utue.publikation.seiten	423-429	de_DE
utue.personen.roh	Nazmina, Gul
utue.personen.roh	Khan, Amjad
utue.personen.roh	Jiang, Jiuhong
utue.personen.roh	Miao, Zhichao
utue.personen.roh	Khan, Shahid Niaz
utue.personen.roh	Khan, Muhammad Ismail
utue.personen.roh	Shah, Abdul Haleem
utue.personen.roh	Shah, Aysha Haleem
utue.personen.roh	Khisroon, Muhammad
utue.personen.roh	Haack, Tobias B.
dcterms.isPartOf.ZSTitelID	Clinical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	4	de_DE
dcterms.isPartOf.ZS-Volume	105	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE