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Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene

ChromatinMendelian DisorderCytogeneticsGenetic DisorderGeneticsMb FragmentPathologyChromosome BiologyMolecular GeneticsCol4a5 GeneChromosomal RearrangementGenomicsAlport SyndromeMedicineChromosome 9