Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families von Wakil, Salma M., Binamer, Yousef, Al-Dossari, Haya, Al-Humaidy, Rawan, Thuraya, Rula Al, Khalifa, Ola, Finsterer, Josef, Meyer, Brian F., Al Owain, Mohammed

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Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene von Meyer, Brian F., Bohlega, Said A., Al-Muhaizea, Mohamed A., Ramzan, Khushnooda, Al Qahtani, Aisha, Finsterer, Josef, Al-Ajlan, Fahad, Hagos, Samya, Monies, Dorota, Wakil, Salma M., Al Humaidy, Rawan

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Novel mutations in TGM 1 and ABCA 12 cause autosomal recessive congenital ichthyosis in five Saudi families von Wakil, Salma M., Binamer, Yousef, Al‐Dossari, Haya, Al‐Humaidy, Rawan, Thuraya, Rula Al, Khalifa, Ola, Finsterer, Josef, Meyer, Brian F., Al Owain, Mohammed

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Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene von Wakil, Salma M, Monies, Dorota, Hagos, Samya, Al-Ajlan, Fahad, Finsterer, Josef, Al Qahtani, Aisha, Ramzan, Khushnooda, Al Humaidy, Rawan, Al-Muhaizea, Mohamed A, Meyer, Brian, Bohlega, Saeed A

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