Elevated Plasma X-Linked Neuroligin 4 Expression Is Associated with Autism Spectrum Disorder

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Elevated Plasma X-Linked Neuroligin 4 Expression Is Associated with Autism Spectrum Disorder ; volume:29 ; number:5 ; year:2020 ; pages:480-485
Medical principles and practice ; 29, Heft 5 (2020), 480-485

Creator: Al-Ayadhi, Laila Y.
Qasem, Hanan Y.
Alghamdi, Hend Ali M.
Elamin, Nadra E.

DOI: 10.1159/000507081

URN: urn:nbn:de:101:1-2020091700210579130398

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:48 AM CEST

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Al-Ayadhi, Laila Y.
Qasem, Hanan Y.
Alghamdi, Hend Ali M.
Elamin, Nadra E.

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Elevated Plasma X-Linked Neuroligin 4 Expression Is Associated with Autism Spectrum Disorder

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Other Objects (12)

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder

Easily misdiagnosed X-linked adrenoleukodystrophy

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

X-linked disorders with cerebellar dysgenesis

X-linked SCID with a rare mutation

Autism spectrum disorder

X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects

X-linked Hyper-IgM Syndrome with Bronchiectasis

Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism

Germline mosaicism in X-linked periventricular nodular heterotopia

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Easily misdiagnosed X-linked adrenoleukodystrophy

Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

X-linked disorders with cerebellar dysgenesis

X-linked SCID with a rare mutation

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Easily misdiagnosed X-linked adrenoleukodystrophy

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Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

X-linked disorders with cerebellar dysgenesis

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Autism spectrum disorder

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X-linked Hyper-IgM Syndrome with Bronchiectasis

Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism

Germline mosaicism in X-linked periventricular nodular heterotopia

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