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Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Document Type

Letter

Author

Faridi, R.; Friedman, T.B.; Stratton, P.; Salmeri, N.; Morell, R.J.; Khan, A.A.; Usmani, M.A.; Riazuddin, S.; Newman, W.G.

Source

In: Clinical Genetics. (Clinical Genetics, May 2024, 105(5):584-586)

Subject

Language

English

ISSN

13990004
00099163

Online Access

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

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