Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)

Ghasemi, Mohammad-Reza; Fateh, Sahand Tehrani; Ben-Mahmoud, Afif; Gupta, Vijay; Stuhn, Lara G.; Lesca, Gaetan; Chatron, Nicolas; Platzer, Konrad; Edery, Patrick; Sadeghi, Hossein; Isidor, Bertrand; Cogne, Benjamin; Schulz, Heidi L.; Krauspe-Stubecke, Ilona; Periyasamy, Radhakrishnan; Nampoothiri, Sheela; Mirfakhraie, Reza; Alijanpour, Sahar; Syrbe, Steffen; Pfeifer, Ulrich; Spranger, Stephanie; Grundmann-Hauser, Kathrin; Haack, Tobias B.; Papadopoulou, Maria T.; da Silva Goncalves, Tayrine; Panagiotakaki, Eleni; Arzimanoglou, Alexis; Tonekaboni, Seyed Hassan; Rossi, Massimiliano; Korenke, G. Christoph; Lacassie, Yves; Jang, Mi-Hyeon; Layman, Lawrence C.; Miryounesi, Mohammad; Kim, Hyung-Goo

dc.contributor.author	Grundmann-Hauser, Kathrin
dc.contributor.author	Stühn, Lara
dc.contributor.author	Haack, Tobias
dc.date.accessioned	2026-01-23T13:59:22Z
dc.date.available	2026-01-23T13:59:22Z
dc.date.issued	2025
dc.identifier.issn	1552-4825
dc.identifier.uri	http://hdl.handle.net/10900/174256
dc.language.iso	en	de_DE
dc.publisher	Hoboken : Wiley	de_DE
dc.relation.uri	http://dx.doi.org/10.1002/ajmg.a.63963	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)	de_DE
dc.type	Article	de_DE
utue.quellen.id	20250630000000_02417
utue.personen.roh	Ghasemi, Mohammad-Reza
utue.personen.roh	Fateh, Sahand Tehrani
utue.personen.roh	Ben-Mahmoud, Afif
utue.personen.roh	Gupta, Vijay
utue.personen.roh	Stuhn, Lara G.
utue.personen.roh	Lesca, Gaetan
utue.personen.roh	Chatron, Nicolas
utue.personen.roh	Platzer, Konrad
utue.personen.roh	Edery, Patrick
utue.personen.roh	Sadeghi, Hossein
utue.personen.roh	Isidor, Bertrand
utue.personen.roh	Cogne, Benjamin
utue.personen.roh	Schulz, Heidi L.
utue.personen.roh	Krauspe-Stubecke, Ilona
utue.personen.roh	Periyasamy, Radhakrishnan
utue.personen.roh	Nampoothiri, Sheela
utue.personen.roh	Mirfakhraie, Reza
utue.personen.roh	Alijanpour, Sahar
utue.personen.roh	Syrbe, Steffen
utue.personen.roh	Pfeifer, Ulrich
utue.personen.roh	Spranger, Stephanie
utue.personen.roh	Grundmann-Hauser, Kathrin
utue.personen.roh	Haack, Tobias B.
utue.personen.roh	Papadopoulou, Maria T.
utue.personen.roh	da Silva Goncalves, Tayrine
utue.personen.roh	Panagiotakaki, Eleni
utue.personen.roh	Arzimanoglou, Alexis
utue.personen.roh	Tonekaboni, Seyed Hassan
utue.personen.roh	Rossi, Massimiliano
utue.personen.roh	Korenke, G. Christoph
utue.personen.roh	Lacassie, Yves
utue.personen.roh	Jang, Mi-Hyeon
utue.personen.roh	Layman, Lawrence C.
utue.personen.roh	Miryounesi, Mohammad
utue.personen.roh	Kim, Hyung-Goo
dcterms.isPartOf.ZSTitelID	American Journal of Medical Genetics Part A	de_DE
dcterms.isPartOf.ZS-Issue	5	de_DE
dcterms.isPartOf.ZS-Volume	197	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE