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Leukodystrophy with disorders of sex development due to WT1 mutations.

Paulo Victor Sgobbi Souza | Bruno Mattos Lombardi Badia | Luiz Henrique Libardi Silva | Carlos Alberto Castro Teixeira | Daniel Delgado Seneor | Vitor Dias Gomes Barrios Marin | Igor Braga Farias | Renan Braido Dias | Acary Souza Bulle Oliveira | Wladimir Bocca Vieira Rezende Pinto
Journal of the neurological sciences | 2018

Hypomyelinating leukodystrophies represent an expanding group of neurogenetic disorders characterized primarily by central nervous system hypomyelination and variable neurological and non-neurological involvement. Hypomyelinating disorders have been rarely associated with gonadal dysfunction, being mainly represented by hypogonadotrophic hypogonadism in 4H syndrome. WT1 gene-associated disorders are classically associated with complex phenotypes including early carcinogenic risk for gonadoblastoma and Wilms' tumor, chronic renal failure, nephrotic syndrome and sex developmental disorders in intersex disorders and ambiguous genitalia.

Pubmed ID: 29801916

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SAMTOOLS (tool)

RRID:SCR_002105

Original SAMTOOLS package has been split into three separate repositories including Samtools, BCFtools and HTSlib. Samtools for manipulating next generation sequencing data used for reading, writing, editing, indexing,viewing nucleotide alignments in SAM,BAM,CRAM format. BCFtools used for reading, writing BCF2,VCF, gVCF files and calling, filtering, summarising SNP and short indel sequence variants. HTSlib used for reading, writing high throughput sequencing data.

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