<i>LINS1</i>-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrum.

Neuhofer, Christiane M; Catarino, Claudia B; Schmidt, Heinrich; Seelos, Klaus; Alhaddad, Bader; Haack, Tobias B; Klopstock, Thomas

LINS1-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrum.

Neuhofer, Christiane M; Catarino, Claudia B; Schmidt, Heinrich; Seelos, Klaus; Alhaddad, Bader; Haack, Tobias B; Klopstock, Thomas.

Afiliación

Neuhofer CM; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp
Catarino CB; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp
Schmidt H; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp
Seelos K; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp
Alhaddad B; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp
Haack TB; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp
Klopstock T; Friedrich-Baur-Institute (C.M.N., C.B.C., T.K.), Department of Neurology, University Hospital, LMU Munich, Germany; Institute of Human Genetics (C.M.N.), University Medical Center Göttingen, Germany; Department of Pediatrics (H.S.), Medical Genetics, Dr. von Haunersches Kinderspital, University Hosp

Neurol Genet ; 6(5): e500, 2020 Oct.

Article en En | MEDLINE | ID: mdl-32802957

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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Neurol Genet Año: 2020 Tipo del documento: Article