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A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins

Document Type

Article

Author

Paganini, L.; Bonaparte, E.; Tabano, S.M.; Costanza, J.; Miozzo, M.; Fontana, L.; Colapietro, P.; Hadi, L.A.; Riboni, L.; Chetta, M.; Rovina, D.; Sirchia, S.M.; Pezzani, L.; Marchisio, P.; Milani, D.

Source

In: Clinical Genetics. (Clinical Genetics, March 2019, 95(3):368-374)

Subject

Language

English

ISSN

13990004
00099163

Online Access

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