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Familial spastic paraparesis syndrome associated with HTLV-I infection.
Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes.
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Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ.
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LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ.
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ. Neurology. 2001 Aug 14; 57(3):416-22.
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PubMed
subject areas
1-Alkyl-2-acetylglycerophosphocholine Esterase
Brain
Brain Diseases
Child
Child, Preschool
Female
Humans
Infant
Intelligence
Magnetic Resonance Imaging
Male
Microtubule-Associated Proteins
Mutation, Missense
Phenotype
authors with profiles
William B. Dobyns