Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

Author： Kong Xiao-Fei   Vogt Guillaume   Itan Yuval   Macura-Biegun Anna   Szaflarska Anna   Kowalczyk Danuta   Chapgier Ariane   Abhyankar Avinash   Furthner Dieter   Djambas Khayat Claudia   Okada Satoshi   Bryant Vanessa L.   Bogunovic Dusan   Kreins Alexandra   Moncada-Vélez Marcela   Migaud Mélanie   Al-Ajaji Sulaiman   Al-Muhsen Saleh   Holland Steven M.   Abel Laurent   Picard Capucine   Chaussabel Damien   Bustamante Jacinta   Casanova Jean-Laurent   Boisson-Dupuis Stéphanie  

Publisher： Oxford University Press

E-ISSN： 0964-6906|22|4|769-781

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.22, Iss.4, 2013-02, pp. : 769-781

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2

By Hodgkinson C.A.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 703-708

Oxford University Press

Access to resources Recommend Favorite

Mitochondrial Dysfunction in a Patient with 8q21.11 Deletion and Charcot-Marie-Tooth Disease Type 2K due to GDAP1 Haploinsufficiency

By  

Molecular Syndromology, Vol. 6, Iss. 4, 2015-0 ,pp. : 204-206

Karger

Access to resources Recommend Favorite

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome

By Cross Sally H.  

Human Molecular Genetics, Vol. 13, Iss. 14, 2004-07 ,pp. : 1433-1439

Oxford University Press

Access to resources Recommend Favorite

Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders

By  

Current Genomics, Vol. 9, Iss. 3, 2008-05 ,pp. : 137-146

Bentham Science Publishers

Access to resources Recommend Favorite

Linkage of Polymorphic Congenital Cataract to the γ-Crystallin Gene Locus on Human Chromosome 2q33–35

By Rogaev Evgeny I.   Rogaeva Ekaterina A.   Korovaitseva Galina I.   Farrer Lindsay A.   Petrin Alexander N.   Keryanov Sergey A.   Turaeva Shirine   Chumakov Ilya   George-Hyslop Peter St.   Ginter Eugeny K.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 699-703

Oxford University Press

Access to resources Recommend Favorite