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Fungiform Papilla Number and Olfactory Threshold Assessment in Males With and Without Barth Syndrome
Publikováno v:
Chemosensory Perception. 10:60-68
Barth syndrome is a rare X-linked genetic disorder caused by a mutation or deletion of the tafazzin gene. Approximately 50–70% of affected males have family-reported feeding issues that affect eating habits and/or restrict dietary intake. Research
Autor:
Barlow, Kate G., Reynolds, Stacey
Publikováno v:
Open Journal of Occupational Therapy (OJOT); Spring2018, Vol. 6 Issue 2, preceding p1-12, 14p