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Publikováno v:
The FASEB Journal. 36
Publikováno v:
The FASEB Journal. 35
Publikováno v:
Clinical Genetics. 90:263-269
Woodhouse Sakati syndrome (WSS, MIM 241080) is a rare autosomal recessive genetic condition characterized by alopecia, hypogonadism, hearing impairment, diabetes mellitus, learning disabilities and extrapydamidal manifestations. Sequence variants in