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searching for X-linked agammaglobulinemia 7 found (44 total)

alternate case: x-linked agammaglobulinemia

HNRPH2 (780 words) [view diff] exact match in snippet view article find links to article

HNRPH1. This gene is thought to be involved in Fabry disease and X-linked agammaglobulinemia phenotype. Alternative splicing results in multiple transcript

Btk-type zinc finger (651 words) [view diff] exact match in snippet view article find links to article

cellular processes. Mutations affecting Btk are the cause of X-linked agammaglobulinemia (XLA) in humans and X-linked immunodeficiency in mice. Mammalian

IGLL1 (1,148 words) [view diff] exact match in snippet view article find links to article

Kanegane H, Karasuyama H, et al. (2000). "Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later

Ogden Bruton (994 words) [view diff] exact match in snippet view article find links to article

type of agammaglobulinemia is now called Bruton's syndrome or X-linked agammaglobulinemia, which was later found by others to be an X-linked congenital

TIMM8A (1,890 words) [view diff] exact match in snippet view article find links to article

A (June 2016). "Xq22.1 contiguous gene deletion syndrome of X-linked agammaglobulinemia and Mohr-Tranebjærg syndrome". Annals of Allergy, Asthma & Immunology

5'-nucleotidase (1,598 words) [view diff] exact match in snippet view article find links to article

combined immuno-deficiency, Wiskott–Aldrich syndrome, congenital X-linked agammaglobulinemia, selective IgA deficiency and acquired immune deficiency syndrome

Hyaluronidase (3,092 words) [view diff] exact match in snippet view article find links to article

includes, but is not limited to, common variable immunodeficiency, X-linked agammaglobulinemia, congenital agammaglobulinemia, Wiskott-Aldrich syndrome, and