Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report

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Standort: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2350

Umfang: Online-Ressource

Sprache: Englisch

Anmerkungen: online resource.

Erschienen in: Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report ; volume:21 ; number:1 ; day:21 ; month:10 ; year:2020 ; pages:1-7 ; date:12.2020
BMC medical genetics ; 21, Heft 1 (21.10.2020), 1-7, 12.2020

Urheber: Kozina, Anastasiya Aleksandrovna
Okuneva, Elena Grigorievna
Baryshnikova, Natalia Vladimirovna
Fedonyuk, Inessa Dmitrievna
Kholin, Alexey Aleksandrovich
Il’ina, Elena Stepanovna
Krasnenko, Anna Yurievna
Stetsenko, Ivan Fedorovich
Plotnikov, Nikolay Alekseevich
Klimchuk, Olesia Igorevna
Surkova, Ekaterina Ivanovna
Ilinsky, Valery Vladimirovich

Beteiligte Personen und Organisationen: SpringerLink (Online service)

DOI: 10.1186/s12881-020-01119-6

URN: urn:nbn:de:101:1-2020120619540908810247

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

Letzte Aktualisierung: 15.08.2025, 07:38 MESZ

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Beteiligte

Kozina, Anastasiya Aleksandrovna
Okuneva, Elena Grigorievna
Baryshnikova, Natalia Vladimirovna
Fedonyuk, Inessa Dmitrievna
Kholin, Alexey Aleksandrovich
Il’ina, Elena Stepanovna
Krasnenko, Anna Yurievna
Stetsenko, Ivan Fedorovich
Plotnikov, Nikolay Alekseevich
Klimchuk, Olesia Igorevna
Surkova, Ekaterina Ivanovna
Ilinsky, Valery Vladimirovich
SpringerLink (Online service)

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Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report

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