In the article entitled “Expanding the phenotype of DST-related disorder: A case report suggesting a genotype/phenotype correlation” by Cappuccio et al., “c.3886C > T” incorrectly appears as “c.3886A > G” and the “c.806A > G” incorrectly appears as “c.806C > T” both in abstract and in the text. The authors apologize for the error and any inconvenience that might have resulted.
Corrigendum to: Expanding the phenotype of DST -related disorder: A case report suggesting a genotype/phenotype correlation (American Journal of Medical Genetics Part A, (2017), 173, 10, (2743-2746), 10.1002/ajmg.a.38367) / Cappuccio, G.; Pinelli, M.; Torella, A.; Alagia, M.; Auricchio, Renata.; Staiano, A.; Nigro, V.; Brunetti-Pierri, Nicola. - In: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A. - ISSN 1552-4825. - 182:1(2020), pp. 268-268. [10.1002/ajmg.a.61386]
Corrigendum to: Expanding the phenotype of DST -related disorder: A case report suggesting a genotype/phenotype correlation (American Journal of Medical Genetics Part A, (2017), 173, 10, (2743-2746), 10.1002/ajmg.a.38367)
Cappuccio G.;Pinelli M.;Alagia M.;Auricchio Renata.;Staiano A.;Brunetti-Pierri Nicola
2020
Abstract
In the article entitled “Expanding the phenotype of DST-related disorder: A case report suggesting a genotype/phenotype correlation” by Cappuccio et al., “c.3886C > T” incorrectly appears as “c.3886A > G” and the “c.806A > G” incorrectly appears as “c.806C > T” both in abstract and in the text. The authors apologize for the error and any inconvenience that might have resulted.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
