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Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 gene. [electronic resource] by
- Hartikainen, J M
- Ju, W
- Wisniewski, K E
- Moroziewicz, D N
- Kaczmarski, A L
- McLendon, L
- Zhong, D
- Suarez, C T
- Brown, W T
- Zhong, N
Producer: 19990712
In:
Molecular genetics and metabolism vol. 67
Availability: No items available.
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12.
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Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene. [electronic resource] by
- Zhong, N
- Wisniewski, K E
- Kaczmarski, A L
- Ju, W
- Xu, W M
- Xu, W W
- Mclendon, L
- Liu, B
- Kaczmarski, W
- Sklower Brooks, S S
- Brown, W T
Producer: 19980303
In:
Human genetics vol. 102
Availability: No items available.
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13.
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Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis. [electronic resource] by
- Wisniewski, K E
- Zhong, N
- Kaczmarski, W
- Kaczmarski, A
- Kida, E
- Brown, W T
- Schwarz, K O
- Lazzarini, A M
- Rubin, A J
- Stenroos, E S
- Johnson, W G
- Wisniewski, T M
Producer: 19980217
In:
Annals of neurology vol. 43
Availability: No items available.
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