Mutations in the histamine N-methyltransferase gene, HNMT, are associated with non-syndromic autosomal recessive intellectual disability

Abolfazl Heidari; Chanakan Tongsook; Reza Najafipour; Luciana Musante; Nasium Vasli; Masoud Garshasbi; Hao Hu; Kirti Mittal; Amy McNaughton; Kumudesh Sritharan; Melissa Hudson; Henning Stehr; Saeid Talebi; Mohammad Moradi; Hossein Darvish; Muhammad Arshad Rafiq; Hossein Mozhdehipanah; Christian Windpassinger; Gabriele Gillessen-Kaesbach; Andreas Tzschach; Iltaf Ahmed; Anna Mikhailov; James Stavropoulos; Melissa Carter; Soraya Keshavarz; Muhammad Ayub; Hossein Najmabadi; Xudong Liu; Hans Hilger Ropers; Peter Macheroux; John Vincent

Mutations in the histamine N-methyltransferase gene, HNMT, are associated with non-syndromic autosomal recessive intellectual disability

Abolfazl Heidari, Chanakan Tongsook, Reza Najafipour, Luciana Musante, Nasium Vasli, Masoud Garshasbi, Hao Hu, Kirti Mittal, Amy McNaughton, Kumudesh Sritharan, Melissa Hudson, Henning Stehr, Saeid Talebi, Mohammad Moradi, Hossein Darvish, Muhammad Arshad Rafiq, Hossein Mozhdehipanah, Christian Windpassinger, Gabriele Gillessen-Kaesbach, Andreas TzschachIltaf Ahmed, Anna Mikhailov, James Stavropoulos, Melissa Carter, Soraya Keshavarz, Muhammad Ayub, Hossein Najmabadi, Xudong Liu, Hans Hilger Ropers, Peter Macheroux, John Vincent

Institut für Biochemie (6480)

Publikation: Beitrag in einer Fachzeitschrift › Artikel › Begutachtung

Originalsprache	englisch
Seiten (von - bis)	5697-5710
Fachzeitschrift	Human Molecular Genetics
Jahrgang	24
Ausgabenummer	20
Publikationsstatus	Veröffentlicht - 2015

Fields of Expertise

Human- & Biotechnology

Treatment code (Nähere Zuordnung)

Basic - Fundamental (Grundlagenforschung)

Dieses zitieren

Heidari, A., Tongsook, C., Najafipour, R., Musante, L., Vasli, N., Garshasbi, M., Hu, H., Mittal, K., McNaughton, A., Sritharan, K., Hudson, M., Stehr, H., Talebi, S., Moradi, M., Darvish, H., Rafiq, M. A., Mozhdehipanah, H., Windpassinger, C., Gillessen-Kaesbach, G., ... Vincent, J. (2015). Mutations in the histamine N-methyltransferase gene, HNMT, are associated with non-syndromic autosomal recessive intellectual disability. Human Molecular Genetics, 24(20), 5697-5710.

Heidari, A, Tongsook, C, Najafipour, R, Musante, L, Vasli, N, Garshasbi, M, Hu, H, Mittal, K, McNaughton, A, Sritharan, K, Hudson, M, Stehr, H, Talebi, S, Moradi, M, Darvish, H, Rafiq, MA, Mozhdehipanah, H, Windpassinger, C, Gillessen-Kaesbach, G, Tzschach, A, Ahmed, I, Mikhailov, A, Stavropoulos, J, Carter, M, Keshavarz, S, Ayub, M, Najmabadi, H, Liu, X, Ropers, HH, Macheroux, P & Vincent, J 2015, 'Mutations in the histamine N-methyltransferase gene, HNMT, are associated with non-syndromic autosomal recessive intellectual disability', Human Molecular Genetics, Jg. 24, Nr. 20, S. 5697-5710.

@article{4d559cf9edcd4da0acafde89f4e88b21,

title = "Mutations in the histamine N-methyltransferase gene, HNMT, are associated with non-syndromic autosomal recessive intellectual disability",

author = "Abolfazl Heidari and Chanakan Tongsook and Reza Najafipour and Luciana Musante and Nasium Vasli and Masoud Garshasbi and Hao Hu and Kirti Mittal and Amy McNaughton and Kumudesh Sritharan and Melissa Hudson and Henning Stehr and Saeid Talebi and Mohammad Moradi and Hossein Darvish and Rafiq, {Muhammad Arshad} and Hossein Mozhdehipanah and Christian Windpassinger and Gabriele Gillessen-Kaesbach and Andreas Tzschach and Iltaf Ahmed and Anna Mikhailov and James Stavropoulos and Melissa Carter and Soraya Keshavarz and Muhammad Ayub and Hossein Najmabadi and Xudong Liu and Ropers, {Hans Hilger} and Peter Macheroux and John Vincent",

year = "2015",

language = "English",

volume = "24",

pages = "5697--5710",

journal = "Human Molecular Genetics",

issn = "1460-2083",

publisher = "Oxford University Press",

number = "20",

}

TY - JOUR

T1 - Mutations in the histamine N-methyltransferase gene, HNMT, are associated with non-syndromic autosomal recessive intellectual disability

AU - Heidari, Abolfazl

AU - Tongsook, Chanakan

AU - Najafipour, Reza

AU - Musante, Luciana

AU - Vasli, Nasium

AU - Garshasbi, Masoud

AU - Hu, Hao

AU - Mittal, Kirti

AU - McNaughton, Amy

AU - Sritharan, Kumudesh

AU - Hudson, Melissa

AU - Stehr, Henning

AU - Talebi, Saeid

AU - Moradi, Mohammad

AU - Darvish, Hossein

AU - Rafiq, Muhammad Arshad

AU - Mozhdehipanah, Hossein

AU - Windpassinger, Christian

AU - Gillessen-Kaesbach, Gabriele

AU - Tzschach, Andreas

AU - Ahmed, Iltaf

AU - Mikhailov, Anna

AU - Stavropoulos, James

AU - Carter, Melissa

AU - Keshavarz, Soraya

AU - Ayub, Muhammad

AU - Najmabadi, Hossein

AU - Liu, Xudong

AU - Ropers, Hans Hilger

AU - Macheroux, Peter

AU - Vincent, John

PY - 2015

Y1 - 2015

M3 - Article

SN - 1460-2083

VL - 24

SP - 5697

EP - 5710

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 20

ER -