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

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2040-2392

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder ; volume:3 ; number:1 ; day:28 ; month:9 ; year:2012 ; pages:1-12 ; date:12.2012
Molecular autism ; 3, Heft 1 (28.9.2012), 1-12, 12.2012

Creator: Steinberg, Karyn Meltz
Ramachandran, Dhanya
Patel, Viren C.
Shetty, Amol C.
Cutler, David J.
Zwick, Michael E.

Contributor: SpringerLink (Online service)

DOI: 10.1186/2040-2392-3-8

URN: urn:nbn:de:101:1-2021090319191643823610

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

Last update: 15.08.2025, 7:35 AM CEST

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Steinberg, Karyn Meltz
Ramachandran, Dhanya
Patel, Viren C.
Shetty, Amol C.
Cutler, David J.
Zwick, Michael E.
SpringerLink (Online service)

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

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Other Objects (12)

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X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males

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X-linked disorders with cerebellar dysgenesis

X-linked SCID with a rare mutation

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