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Results 1 - 10 of 200 for Gas
  1. ... 6-sulfate sulfatase GALNAC6S galNAc6S sulfatase GALNS_HUMAN GAS MPS4A N-acetylgalactosamine-6-sulfatase N-acetylgalactosamine-6- ...
  2. ... not show signs and symptoms of the condition. GA I Glutaric acidemia I Glutaric acidemia type 1 ...
  3. ... ETFA deficiency ETFB deficiency ETFDH deficiency Ethylmalonic-adipicaciduria GA II Glutaric acidemia, type 2 Glutaric aciduria, type ...
  4. ... of YUHAL syndrome. More About This Health Condition GAS-3 GAS3 growth arrest-specific 3 HNPP MGC20769 ...
  5. Vitelliform macular dystrophy is a genetic eye disorder that can cause worsening (progressive) vision loss. This disorder affects the retina, the specialized light- ...
  6. ... JL, Robitaille YO, Richardson J, Dion PA, Rouleau GA, Shekarabi M. KCC3 axonopathy: neuropathological features in the ... PubMed Dupre N, Bouchard JP, Brais B, Rouleau GA. Hereditary ataxia, spastic paraparesis and neuropathy in the ...
  7. ... E, Joober R, Marineau C, Drapeau P, Rouleau GA. Novel de novo SHANK3 mutation in autistic patients. ... A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, ...
  8. ... PHYTANOYL-CoA HYDROXYLASE; PHYH NCBI Gene ClinVar Jansen GA, Hogenhout EM, Ferdinandusse S, Waterham HR, Ofman R, ... hmg/9.8.1195. Citation on PubMed Jansen GA, Ofman R, Ferdinandusse S, Ijlst L, Muijsers AO, ...
  9. ... YP, Younghusband HB, Hayden MR, Sherrington R, Rouleau GA, Samuels ME. Identification of a novel gene (HSN2) ... AM, Baets J, Houlden H, Brais B, Nicholson GA, Van Esch H, Nafissi S, De Jonghe P, ...
  10. ... N, Dichgans J, Ohkuma A, Siegel AM, Rouleau GA. Linkage to the CCM2 locus and genetic heterogeneity ... M, Maglione V, Squitieri F, Johnson EW, Rouleau GA, Ptacek L, Marchuk DA. Mutations in a gene ...
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