Searching for human epilepsy genes: a progress report.

about

Ion channels and the genetic contribution to epilepsy.

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P2860

Searching for human epilepsy genes: a progress report.

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http://www.wikidata.org/entity/Q40807298

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1993 nî lūn-bûn

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1993年の論文

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1993年論文

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1993年論文

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1993年論文

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1993年論文

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1993年論文

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1993年论文

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1993年论文

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1993年论文

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name

Searching for human epilepsy genes: a progress report.

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Searching for human epilepsy genes: a progress report.

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Searching for human epilepsy genes: a progress report.

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Searching for human epilepsy genes: a progress report

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Andermann E

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Bjerre I

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Connolly M

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Leppert M

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McMahon WM

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Quattlebaum TG

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Rosales TO

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Shevell MI

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Zonana J

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Chromosomal localization of seven neuronal nicotinic acetylcholine receptor subunit genes in humans

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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

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357-369

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scholarly article

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10.1111/J.1750-3639.1993.TB00764.X

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Gabriel M Ronen

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1993-10-01T00:00:00Z

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8293192

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Searching for human epilepsy genes: a progress report.

about

P2860

P2860

Searching for human epilepsy genes: a progress report.

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P1433

P1476

P2093

P2860

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P2860

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P50

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P698