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"name": "Hydrocephalus-inducing-like",
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{
"text": "<p>Hydrocephalus-inducing protein (Hydin) is required for ciliary motility [[cite:PUB00078384]]. Hydin mutations have been shown to associate with primary ciliary dyskinesia in humans [[cite:PUB00078385]].</p>",
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"title": "Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.",
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"Werner C",
"Onoufriadis A",
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"Raidt J",
"Banki NF",
"Shoemark A",
"Burgoyne T",
"Al Turki S",
"Hurles ME; UK10K Consortium",
"Kohler G",
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"Nielsen KG",
"Mitchison HM",
"Omran H",
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"Floyd J",
"Foley R",
"Franklin C",
"Futema M",
"Graham C",
"Humphries S",
"Hurles M",
"Joyce C",
"McCarthy S",
"Mitchison HM",
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"Muntoni F",
"Neil A",
"O'Rahilly S",
"Onoufriadis A",
"Parker V",
"Payne F",
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"Scambler P",
"Schmidts M",
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"Seed M",
"Semple R",
"Serra E",
"Stalker J",
"Van Bockxmeer F",
"van Kogelenberg M",
"Vijayarangakannan P",
"Walter K",
"Whittall R",
"Williamson K",
"Leitersdorf E."
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"title": "Mutations in Hydin impair ciliary motility in mice.",
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"medline_journal": "J Cell Biol",
"ISO_journal": "J. Cell Biol.",
"authors": [
"Lechtreck KF",
"Delmotte P",
"Robinson ML",
"Sanderson MJ",
"Witman GB."
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