The role of MAGT1 in genetic syndromes

Magnesium Research

Volumn 28, Issue 2, 2015, Pages 46-

  Trapani, Valentina ^a   Shomer, Naomi ^b   Rajcan Separovic, Evica ^b  

^a CATHOLIC UNIVERSITY   (Italy)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Immune system; Intellectual disability; Magnesium; Skin; XMEN

Indexed keywords

ARTICLE; COPY NUMBER VARIATION; EPSTEIN BARR VIRUS INFECTION; GENE; GENE MUTATION; GENETIC DISORDER; HOMEOSTASIS; HUMAN; IMMUNE DEFICIENCY; IMMUNE RESPONSE; INTELLECTUAL IMPAIRMENT; MAGT1 GENE; MENTAL RETARDATION MALFORMATION SYNDROME; MINERAL SUPPLEMENTATION; NEOPLASM; NONHUMAN; SKIN DISEASE; X LINKED SEVERE COMBINED IMMUNODEFICIENCY; ANIMAL; GENETICS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INTELLECTUAL DISABILITY; METABOLISM; PHYSIOLOGY; X-LINKED COMBINED IMMUNODEFICIENCY DISEASES;

HUMAN HERPESVIRUS 4;

CATION TRANSPORT PROTEIN; MAGNESIUM; MAGT1 PROTEIN, HUMAN;

ANIMALS; CATION TRANSPORT PROTEINS; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INTELLECTUAL DISABILITY; MAGNESIUM; X-LINKED COMBINED IMMUNODEFICIENCY DISEASES;

EID: 84936802638     PISSN: 09531424     EISSN: 19524021     Source Type: Journal    
DOI: 10.1684/mrh.2015.0381     Document Type: Article

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