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The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD

Document Type

Article

Author

Levy-Khademi, F.; Avnon- Ziv, C.; Lavi, E.; Klopstock, T.; Chertin, B.; Abulibdeh, A.; Levy-Lahad, E.; Zangen, D.; Segel, R.; Zeligson, S.; Renbaum, P.; Rosen, T.; Perlberg-Bengio, S.; Zahdeh, F.; Behar, D.M.

Source

In: Endocrine. (Endocrine, 1 September 2020, 69(3):650-654)

Subject

Language

English

ISSN

15590100
1355008X

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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