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Author/Creator Narkis, Ginat

1. A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers. (8th October 2017)

Authors:
Perez, Yonatan; Wormser, Ohad; Sadaka, Yair; Birk, Ruth; Narkis, Ginat; Birk, Ohad S.
Other Names:
Harrison Paul Academic Editor.
Journal:
BioMed research international
Issue:
Volume 2017(2017)
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Record Type:
Journal Article
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2. Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. Issue 1 (December 2016)

Authors:
Gradstein, Libe; Zolotushko, Jenny; Sergeev, Yuri; Lavy, Itay; Narkis, Ginat; Perez, Yonatan; Guigui, Sarah; Sharon, Dror; Banin, Eyal; Walter, Eyal; Lifshitz, Tova; Birk, Ohad
Journal:
BMC medical genetics
Issue:
Volume 17:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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