Halbritter et al., 2013 - Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. American journal of human genetics   93(5):915-925 Full text @ Am. J. Hum. Genet.
2 Genes / Markers
Marker Type Symbol Name
Gene ift172 intraflagellar transport 172
Gene ift80 intraflagellar transport 80 homolog (Chlamydomonas)
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