Publications by authors named "Almogit Abu"

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Cone-rod dystrophy and a frameshift mutation in the PROM1 gene.
Eran Pras, Almogit Abu, Ygal Rotenstreich, Isaac Avni, Orit Reish

Mol Vis· August 2009

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Clinical disease among patients heterozygous for familial Mediterranean fever.
Dina Marek-Yagel, Yackov Berkun, Shai Padeh, Almogit Abu, Haike Reznik-Wolf

Arthritis Rheum· June 2009

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The D144E substitution in the VSX1 gene: a non-pathogenic variant or a disease causing mutation?
Pras Eran, Abu Almogit, Zadok David, Haike Reznik Wolf, Garzozi Hana

Ophthalmic Genet· June 2008

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Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome.
Almogit Abu, Moshe Frydman, Dina Marek, Eran Pras, Uri Nir

Am J Hum Genet· May 2008

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Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.
Almogit Abu, Moshe Frydman, Dina Marek, Eran Pras, Chaim Stolovitch

Invest Ophthalmol Vis Sci· December 2006

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An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis.
Abraham Zlotogorski, Dina Marek, Liran Horev, Almogit Abu, Dan Ben-Amitai

J Invest Dermatol· June 2006

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