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A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy

Document Type

Article

Author

Shishido, A.; Morisada, N.; Nozu, K.; Iijima, K.; Tominaga, K.; Uemura, H.; Haruna, A.; Hanafusa, H.

Source

In: Human Genome Variation. (Human Genome Variation, 1 December 2020, 7(1))

Subject

Language

English

ISSN

2054345X

Online Access

Full Text (ProQuest Central) JCR 저널정보 Scopus Find it@PNU

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