. "Janda, Ale\u0161" . . "\u0160ediv\u00E1, Anna" . . . . . "15"^^ . "Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes" . "Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes"@en . "X-linked agammaglobulinemia (XLA) is characterized by low levels of B-lymphocytes with early-onset, recurrent, microbial infections occasionally causing neurological symptoms. We observed an atypical clinical course of XLA, complicated since early childh" . "P(1M0520), Z(MSM0021620812)" . "Kontinu\u00E1ln\u00ED delece zahrnuj\u00EDc\u00ED geny BTK, TIMM8A, TAF7L a DRP2"@cs . . . "7"^^ . "X-linked agammaglobulinemia (XLA); Bruton tyrosine kinase (BTK); Mohr-Tranebjaerg syndrome; immunodeficiency; sensorineural deafness; recessive deafness syndrome; brutons tyrosine kinase; linked agammaglobulinemia; mental deficiency; ddp1/timm8a-timm13 complex; dystonia syndrome; ddp gene; mutation; family; expression"@en . "RIV/00064203:_____/07:1587" . "US - Spojen\u00E9 st\u00E1ty americk\u00E9" . "Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes"@en . . . . . "X-linked agammaglobulinemia (XLA) is characterized by low levels of B-lymphocytes with early-onset, recurrent, microbial infections occasionally causing neurological symptoms. We observed an atypical clinical course of XLA, complicated since early childh"@en . . . . . . . "6" . "Journal of Clinical Immunology" . "2"^^ . "0271-9142" . "640-646" . "[F124C3999CE4]" . . "27" . . . "Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes" . . "RIV/00064203:_____/07:1587!RIV08-MSM-00064203" . . . . . "Kontinu\u00E1ln\u00ED delece zahrnuj\u00EDc\u00ED geny BTK, TIMM8A, TAF7L a DRP2"@cs . . . "414923" . . "Popis rozs\u00E1hl\u00E9 delece na X chromozomu, kter\u00E1 vysv\u011Btluje komplexn\u00ED mnoho\u010Detn\u00E1 posti\u017Een\u00ED u pacient\u016F s Brutonovou agamagloublin\u00E9mi\u00ED"@cs . .