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Novel PHEX gene locus-specific database: Comprehensive characterization of vast number of variants associated with X-linked hypophosphatemia (XLH)

Document Type

Article

Author

Sarafrazi, S.; Daugherty, S.C.; Miller, N.; Boada, P.; Dill, K.; Eisenbeis, S.; Krolczyk, S.; Ramesan, P.; Carpenter, T.O.; Chunn, L.; Kiel, M.J.; Econs, M.J.; Imel, E.A.; Johnson, B.; Truty, R.; Sabbagh, Y.

Source

In: Human Mutation. (Human Mutation, February 2022, 43(2):143-157)

Subject

Language

English

ISSN

10981004
10597794

Online Access

Full Text (Wiley Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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