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Two novel POC1A mutations in the primordial dwarfism, SOFT syndrome: Clinical homogeneity but also unreported malformations

Document Type

Article

Author

Barraza-García, J.; Rivera-Pedroza, C.I.; Belinchón, A.; Sentchordi-Montané, L.; del Pozo, A.; Santos-Simarro, F.; Campos-Barros, A.; Lapunzina, P.; García-Miñaur, S.; Heath, K.E.; López-González, V.; Guillén-Navarro, E.; González-Casado, I.; Salamanca, L.

Source

In: American Journal of Medical Genetics, Part A. (American Journal of Medical Genetics, Part A, 1 January 2016, 170(1):210-216)

Subject

Language

English

ISSN

15524833
15524825

Online Access

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

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