Genetics and genomic medicine in Tunisia.

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Genetics and genomic medicine in Tunisia.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Genetics and genomic medicine in Tunisia.

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Genetics and genomic medicine in Tunisia.

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Genetics and genomic medicine in Tunisia.

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Genetics and genomic medicine in Tunisia.

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Genetics and genomic medicine in Tunisia.

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Genetics and genomic medicine in Tunisia.

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P1476

Genetics and genomic medicine in Tunisia.

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P2093

Habiba Chaabouni Bouhamed

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Houda Elloumi-Zghal

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P2860

Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma

A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa.

North African Jewish and non-Jewish populations form distinctive, orthogonal clusters

Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins

CTGA: the database for genetic disorders in Arab populations

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134-159

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scholarly article

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10.1002/MGG3.392

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2018-03-01T00:00:00Z

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29663716

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5902400

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