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The adrenoleukodystrophy database serves as a catalog for ABCD1 mutations and provides information on X-ALD.

Provide information about genetic variation of the alpl gene responsible for hypophosphatasia. Includes a downloadable list of genotypes and mutations .

Searchable database of known and novel MECP2 disease-causing mutations and polymorphisms. From the International Rett Syndrome Association.

Provide up-to-date information about genetic variation of the adenylosuccinate lyase gene. Includes cDNA sequence and gene structure.

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GenomeNet is a Japanese network of database and computational services for genome research and related research areas in biomedical sciences.

Live what you love (by Daina)

ORNL conducts basic and applied research and development to create scientific knowledge and technological solutions.