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

A Heidari; C Tongsook; R Najafipour; L Musante; N Vasli; M Garshasbi; H Hu; K Mittal; AJ McNaughton; K Sritharan; M Hudson; H Stehr; S Talebi; M Moradi; H Darvish; M Arshad Rafiq; H Mozhdehipanah; A Rashidinejad; S Samiei; M Ghadami; Christian Windpassinger; G Gillessen-Kaesbach; A Tzschach; I Ahmed; A Mikhailov; DJ Stavropoulos; MT Carter; S Keshavarz; M Ayub; H Najmabadi; X Liu; HH Ropers; P Macheroux; JB Vincent

doi:10.1093/hmg/ddv286

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

A Heidari
, C Tongsook
, R Najafipour
, L Musante
, N Vasli
, M Garshasbi
, H Hu
, K Mittal
, AJ McNaughton
, K Sritharan
, M Hudson
, H Stehr
, S Talebi
, M Moradi
, H Darvish
, M Arshad Rafiq
, H Mozhdehipanah
, A Rashidinejad
, S Samiei
, M Ghadami

Christian Windpassinger, G Gillessen-Kaesbach, A Tzschach, I Ahmed, A Mikhailov, DJ Stavropoulos, MT Carter, S Keshavarz, M Ayub, H Najmabadi, X Liu, HH Ropers, P Macheroux, JB Vincent

Diagnostik- & Forschungsinstitut für Humangenetik

Publikation: Beitrag in Fachzeitschrift › Originalarbeit

25 Quellenangaben (Web of Science)

Originalsprache	Englisch
Fachzeitschrift	Human Molecular Genetics
DOIs	https://doi.org/10.1093/hmg/ddv286
Publikationsstatus	Veröffentlicht - 2015

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305 Andere Humanmedizin, Gesundheitswissenschaften

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Neurowissenschaften

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10.1093/hmg/ddv286

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Heidari, A., Tongsook, C., Najafipour, R., Musante, L., Vasli, N., Garshasbi, M., Hu, H., Mittal, K., McNaughton, AJ., Sritharan, K., Hudson, M., Stehr, H., Talebi, S., Moradi, M., Darvish, H., Arshad Rafiq, M., Mozhdehipanah, H., Rashidinejad, A., Samiei, S., ... Vincent, JB. (2015). Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddv286

@article{c83cea7e2f28439db8916b276852dccc,

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

author = "A Heidari and C Tongsook and R Najafipour and L Musante and N Vasli and M Garshasbi and H Hu and K Mittal and AJ McNaughton and K Sritharan and M Hudson and H Stehr and S Talebi and M Moradi and H Darvish and \{Arshad Rafiq\}, M and H Mozhdehipanah and A Rashidinejad and S Samiei and M Ghadami and Christian Windpassinger and G Gillessen-Kaesbach and A Tzschach and I Ahmed and A Mikhailov and DJ Stavropoulos and MT Carter and S Keshavarz and M Ayub and H Najmabadi and X Liu and HH Ropers and P Macheroux and JB Vincent",

year = "2015",

doi = "10.1093/hmg/ddv286",

language = "English",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

}

Heidari, A, Tongsook, C, Najafipour, R, Musante, L, Vasli, N, Garshasbi, M, Hu, H, Mittal, K, McNaughton, AJ, Sritharan, K, Hudson, M, Stehr, H, Talebi, S, Moradi, M, Darvish, H, Arshad Rafiq, M, Mozhdehipanah, H, Rashidinejad, A, Samiei, S, Ghadami, M, Windpassinger, C, Gillessen-Kaesbach, G, Tzschach, A, Ahmed, I, Mikhailov, A, Stavropoulos, DJ, Carter, MT, Keshavarz, S, Ayub, M, Najmabadi, H, Liu, X, Ropers, HH, Macheroux, P & Vincent, JB 2015, 'Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.', Human Molecular Genetics. https://doi.org/10.1093/hmg/ddv286

TY - JOUR

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

AU - Heidari, A

AU - Tongsook, C

AU - Najafipour, R

AU - Musante, L

AU - Vasli, N

AU - Garshasbi, M

AU - Hu, H

AU - Mittal, K

AU - McNaughton, AJ

AU - Sritharan, K

AU - Hudson, M

AU - Stehr, H

AU - Talebi, S

AU - Moradi, M

AU - Darvish, H

AU - Arshad Rafiq, M

AU - Mozhdehipanah, H

AU - Rashidinejad, A

AU - Samiei, S

AU - Ghadami, M

AU - Windpassinger, Christian

AU - Gillessen-Kaesbach, G

AU - Tzschach, A

AU - Ahmed, I

AU - Mikhailov, A

AU - Stavropoulos, DJ

AU - Carter, MT

AU - Keshavarz, S

AU - Ayub, M

AU - Najmabadi, H

AU - Liu, X

AU - Ropers, HH

AU - Macheroux, P

AU - Vincent, JB

PY - 2015

Y1 - 2015

UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000363022600004

UR - https://pubmed.ncbi.nlm.nih.gov/26206890

UR - https://pmc.ncbi.nlm.nih.gov/articles/PMC4581600

U2 - 10.1093/hmg/ddv286

DO - 10.1093/hmg/ddv286

M3 - Research article

C2 - 26206890

SN - 0964-6906

JO - Human Molecular Genetics

JF - Human Molecular Genetics

ER -