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CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report
by
Tolmacheva, Ekaterina R
,
Shubina, Jekaterina
,
Kochetkova, Taisiya O
,
Ushakova, Lubov' V
,
Bokerija, Ekaterina L
,
Vasiliev, Grigory S
,
Mikhaylovskaya, Galina V
,
Atapina, Ekaterina E
,
Zaretskaya, Nadezhda V
,
Sukhikh, Gennady T
,
Rebrikov, Denis V
,
Trofimov, Dmitriy Yu
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Genes
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WES-based screening of 7,000 newborns: A pilot study in Russia
by
Shubina, Jekaterina
,
Tolmacheva, Ekaterina
,
Maslennikov, Dmitry
,
Kochetkova, Taisiya
,
Mukosey, Irina
,
Sadelov, Igor
,
Goltsov, Andrey
,
Barkov, Ilya
,
Ekimov, Aleksey
,
Rogacheva, Margarita
,
Stupko, Olga
,
Pavlova, Nadezhda
,
Kuznetsova, Maria
,
Dokshukina, Alina
,
Vasiliev, Grigory
,
Bolshakova, Anna
,
Kovalskaia, Valeriia
,
Korovko, Anastasia
,
Pomerantseva, Ekaterina
,
Tsabai, Polina
,
Buyanovskaya, Olga
,
Zaretskaya, Nadezhda
,
Karetnikova, Natalia
,
Grebenshchikova, Elena
,
Degtyareva, Anna
,
Bokerija, Ekaterina
,
Kholin, Alexey
,
Rebrikov, Denis
,
Degtyarev, Dmitry
,
Trofimov, Dmitriy
,
Sukhih, Gennady
Published in
HGG advances
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