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KO

Karim Ouahchi

Pathology / Clinical Pathology/Laboratory Medicine

Credentials: ·

Research

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
Nature Genetics · 2001 · 584 citations
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein
Nature Genetics · 1995 · First of 10 authors · 446 citations
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration
The American Journal of Human Genetics · 2008 · 141 citations

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