Suchergebnisse - "Patel, Mitali"

PubPharm (4)

1

Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations

enthalten in: Human molecular genetics | 2023

von Fassad, M. | Rumman, N. | Junger, K. | +8

2

Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia

enthalten in: Clinical genetics | 2020

von Fassad, M. | Shoman, W. | Morsy, H. | +7

3

Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects

enthalten in: Human molecular genetics | 2014

von Onoufriadis, A. | Shoemark, A. | Schmidts, M. | +21

4

Dimerization of complement factor H-related proteins modulates complement activation in vivo

Erschienen: 2013

von de Jorge, E. | Caesar, J. | Malik, T. | +8

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