Your browser doesn't support javascript.
loading
Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene.
Nwebube, Chineze; Bulancea, Sabrina; Marchidann, Adrian; Bello-Espinosa, Lourdes; Treidler, Simona.
Afiliação
  • Nwebube C; Stony Brook University Hospital (C.N., L.B.-E.), NY; Pneumophtisiology Clinical Hospital (S.B.), Brasov, Romania; Kings County Hospital (A.M.), Brooklyn, NY; and SUNY Downstate (S.T.), Maimonides Medical Center, Brooklyn.
  • Bulancea S; Stony Brook University Hospital (C.N., L.B.-E.), NY; Pneumophtisiology Clinical Hospital (S.B.), Brasov, Romania; Kings County Hospital (A.M.), Brooklyn, NY; and SUNY Downstate (S.T.), Maimonides Medical Center, Brooklyn.
  • Marchidann A; Stony Brook University Hospital (C.N., L.B.-E.), NY; Pneumophtisiology Clinical Hospital (S.B.), Brasov, Romania; Kings County Hospital (A.M.), Brooklyn, NY; and SUNY Downstate (S.T.), Maimonides Medical Center, Brooklyn.
  • Bello-Espinosa L; Stony Brook University Hospital (C.N., L.B.-E.), NY; Pneumophtisiology Clinical Hospital (S.B.), Brasov, Romania; Kings County Hospital (A.M.), Brooklyn, NY; and SUNY Downstate (S.T.), Maimonides Medical Center, Brooklyn.
  • Treidler S; Stony Brook University Hospital (C.N., L.B.-E.), NY; Pneumophtisiology Clinical Hospital (S.B.), Brasov, Romania; Kings County Hospital (A.M.), Brooklyn, NY; and SUNY Downstate (S.T.), Maimonides Medical Center, Brooklyn.
Neurol Genet ; 7(2): e570, 2021 Apr.
Article em En | MEDLINE | ID: mdl-33688580

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Neurol Genet Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Neurol Genet Ano de publicação: 2021 Tipo de documento: Article