Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp-Reference-Cited by-同舟云学术

Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp

Author:

Bertola Débora¹²^ORCID,Buscarilli Michelle¹,Stabley Deborah L.³,Baker Laura⁴,Doyle Daniel⁵,Bartholomew Dennis W.⁶,Sol‐Church Katia³,Gripp Karen W.³⁴

Affiliation:

1. Unidade de Genética ClínicaInstituto da Criança do Hospital das Clínicas da Faculdade de Medicina da Universidade de São PauloSão PauloBrazil

2. Instituto de Biociências da Universidade de São PauloSão PauloBrazil

3. Center for Applied Clinical GenomicsA. I. duPont Hospital for Children/NemoursWilmingtonDelaware

4. Division of Medical GeneticsA. I. duPont Hospital for Children/NemoursWilmingtonDelaware

5. Division of EndocrinologyA. I. duPont Hospital for Children/NemoursWilmingtonDelaware

6. Division of Molecular and Human GeneticsNationwide Children's HospitalColumbusOhio

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

National Institute of General Medical Sciences

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference27 articles.

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